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DisCoVisc Versus DuoVisc, Healon5 and AmVisc Plus

DisCoVisc Versus Competitor

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00712244
Enrollment
112
Registered
2008-07-09
Start date
2007-10-31
Completion date
Unknown
Last updated
2010-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract

Keywords

Discovisc, Ophthalmic Viscosurgical Device

Brief summary

A comparison of the ability of DisCoVisc to that of other ophthalmic viscosurgical devices (OVDs) (DuoVisc, Healon5 or Amvisc PLUS) regarding endothelial protection and anterior chamber space maintenance during non-eventful cataract surgery.

Interventions

DEVICEDisCoVisc

Use of DisCoVisc Ophthalmic Viscosurgical Device (4% sodium chondroitin sulfate, 1.65% sodium hyaluronate) during cataract surgery.

DEVICEDuoVisc

Use of DuoVisc viscoelastic system consisting of Viscoat (3% sodium hyaluronate, 4% chondroitin sulfate)and Provisc(1% sodium hyaluronate) during cataract surgery.

DEVICEHealon5

Use of Healon5 ophthalmic viscosurgical device (2.3% Sodium Hyaluronate) during cataract surgery.

Use of Amvisc Plus ophthalmic viscosurgical device (1.6% Sodium Hyaluronate) during cataract surgery.

Sponsors

Alcon Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* operable cataracts in at least one eye

Exclusion criteria

* Endothelial Cell Count (ECC) ≤1500cells/mm2 * Intraocular Pressure (IOP) \> 21mm Hg * previous ocular inflammation * systemic or ocular conditions affecting corneal endothelium

Design outcomes

Primary

MeasureTime frameDescription
Corneal Endothelial Cell Loss1 month after surgeryPercentage of corneal endothelial cells lost 1 month after surgery as compared to the number of corneal endothelial cells measured before surgery. Corneal endothelial cells are measured by counting the number of cells on an image taken by specular microscope.

Secondary

MeasureTime frameDescription
Percent Gain in Corneal Thickness.1 week and month after surgeryPercent Gain in Corneal Thickness between the assessment performed before surgery to that performed after surgery. This was assessed at both the 1 week and 1 month visit. Corneal thickness is measured in micrometers and is evaluated by Pachymetry. A negative number indicates a decrease in corneal thickness.
Aqueous Signs - Corneal Edema1 day after surgeryMeasured as the percentage of patient's eyes subjectively evaluated to have corneal edema at each of the following gradings: 0 - none; 1 - Mild, slight localized or generalized edema; 2 - Moderate, significant localized or generalized edema; 3 - Severe, advanced localized or generalized edema.
Aqueous Signs - Aqueous Flare1 Day after SurgeryMeasured as the percentage of patient's eyes subjectively evaluated to have Aqueous Flare at each of the following gradings: 0 - None: No visible flare when compared to the normal eye, 1 - Mild: Flare visible against dark papillary background but not visible against iris background, 2 - Moderate: Flare is visible with the slit-lamp beam aimed onto the iris surface as well as teh dark papillary background, 3 - Severe: Very dense flare. May also present as a hazy appearance of anterior segment structures when viewed with low power magnification of the slit-lamp.
Intraocular Pressure (IOP)1 day after surgeryMeasure of intraocular pressure of a patient's eye via tonometry one day after surgery. Measured in mmHg. Normal intraocular pressure is between 10 mmHg and 20 mmHg.
Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyTime of surgerySurgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during anterior capsulotomy. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.
Surgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationTime of SurgerySurgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during phacoemulsification. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.
Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionTime of SurgerySurgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during intraocular lens (IOL) insertion. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.
Aqueous Signs - Aqueous Cells1 day after surgeryMeasured as the percentage of patient's eyes subjectively evaluated to have Aqueous Cells at each of the following gradings: 0 - None, 1 - 1 to 5 cells, 2 - 6 to 15 cells, 3 - 16 - 30 cells, 4 - \>30 cells.

Countries

United States

Participant flow

Recruitment details

Subjects were \>50 years old & of any race & gender. Subjects had operable cataracts in at least 1 eye, were able to provide informed consent, & were free of systemic diseases affecting ocular health, especially those affecting endothelial cell counts. Eyes were free of ocular disease & had no history of chronic/recurrent inflammatory eye disease.

Pre-assignment details

During the preoperative exam, subjects were examined to ensure they met the inclusion/exclusion criteria. Only subjects who signed an informed consent and qualified to be in the study by meeting all inclusion/exclusion criteria were enrolled. Group assignment was based on an Excel randomization scheme.

Participants by arm

ArmCount
DISCOVISC
DISCOVISC® Ophthalmic Viscosurgical Device (OVD)
29
DUOVISC
DUOVISC® Viscoelastic system
29
Healon5
Healon5 Ophthalmic Viscosurgical Device
27
Amvisc Plus
Amvisc Plus Ophthalmic Viscosurgical Device
27
Total112

Baseline characteristics

CharacteristicDISCOVISCDUOVISCHealon5Amvisc PlusTotal
Age Categorical
<=18 years
0 participants0 participants0 participants0 participants0 participants
Age Categorical
>=65 years
16 participants15 participants18 participants18 participants67 participants
Age Categorical
Between 18 and 65 years
12 participants12 participants9 participants8 participants41 participants
Gender
Female
18 participants15 participants16 participants19 participants68 participants
Gender
Male
10 participants12 participants11 participants7 participants40 participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —— / —
other
Total, other adverse events
0 / 290 / 290 / 270 / 27
serious
Total, serious adverse events
0 / 290 / 290 / 270 / 27

Outcome results

Primary

Corneal Endothelial Cell Loss

Percentage of corneal endothelial cells lost 1 month after surgery as compared to the number of corneal endothelial cells measured before surgery. Corneal endothelial cells are measured by counting the number of cells on an image taken by specular microscope.

Time frame: 1 month after surgery

ArmMeasureValue (MEAN)Dispersion
DISCOVISCCorneal Endothelial Cell Loss1.51 Percent ChangeStandard Deviation 5.99
DUOVISCCorneal Endothelial Cell Loss1.18 Percent ChangeStandard Deviation 11.18
Healon5Corneal Endothelial Cell Loss4.72 Percent ChangeStandard Deviation 7.23
Amvisc PlusCorneal Endothelial Cell Loss6.30 Percent ChangeStandard Deviation 14.31
Secondary

Aqueous Signs - Aqueous Cells

Measured as the percentage of patient's eyes subjectively evaluated to have Aqueous Cells at each of the following gradings: 0 - None, 1 - 1 to 5 cells, 2 - 6 to 15 cells, 3 - 16 - 30 cells, 4 - \>30 cells.

Time frame: 1 day after surgery

Population: This data was collected for all subjects attending the visit one day after surgery.

ArmMeasureGroupValue (NUMBER)
DISCOVISCAqueous Signs - Aqueous CellsGrade 224.14 Percentage of participants
DISCOVISCAqueous Signs - Aqueous CellsGrade 33.45 Percentage of participants
DISCOVISCAqueous Signs - Aqueous CellsGrade 06.9 Percentage of participants
DISCOVISCAqueous Signs - Aqueous CellsGrade 165.52 Percentage of participants
DISCOVISCAqueous Signs - Aqueous CellsGrade 40 Percentage of participants
DUOVISCAqueous Signs - Aqueous CellsGrade 232.14 Percentage of participants
DUOVISCAqueous Signs - Aqueous CellsGrade 37.14 Percentage of participants
DUOVISCAqueous Signs - Aqueous CellsGrade 146.43 Percentage of participants
DUOVISCAqueous Signs - Aqueous CellsGrade 014.29 Percentage of participants
DUOVISCAqueous Signs - Aqueous CellsGrade 40 Percentage of participants
Healon5Aqueous Signs - Aqueous CellsGrade 238.46 Percentage of participants
Healon5Aqueous Signs - Aqueous CellsGrade 07.69 Percentage of participants
Healon5Aqueous Signs - Aqueous CellsGrade 150 Percentage of participants
Healon5Aqueous Signs - Aqueous CellsGrade 33.85 Percentage of participants
Healon5Aqueous Signs - Aqueous CellsGrade 40 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous CellsGrade 33.85 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous CellsGrade 165.38 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous CellsGrade 07.69 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous CellsGrade 223.08 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous CellsGrade 40 Percentage of participants
Secondary

Aqueous Signs - Aqueous Flare

Measured as the percentage of patient's eyes subjectively evaluated to have Aqueous Flare at each of the following gradings: 0 - None: No visible flare when compared to the normal eye, 1 - Mild: Flare visible against dark papillary background but not visible against iris background, 2 - Moderate: Flare is visible with the slit-lamp beam aimed onto the iris surface as well as teh dark papillary background, 3 - Severe: Very dense flare. May also present as a hazy appearance of anterior segment structures when viewed with low power magnification of the slit-lamp.

Time frame: 1 Day after Surgery

Population: This data was collected for all subjects attending the visit one day after surgery.

ArmMeasureGroupValue (NUMBER)
DISCOVISCAqueous Signs - Aqueous FlareNone20.69 Percentage of participants
DISCOVISCAqueous Signs - Aqueous FlareMild75.86 Percentage of participants
DISCOVISCAqueous Signs - Aqueous FlareModerate3.45 Percentage of participants
DISCOVISCAqueous Signs - Aqueous FlareSevere0 Percentage of participants
DUOVISCAqueous Signs - Aqueous FlareMild53.57 Percentage of participants
DUOVISCAqueous Signs - Aqueous FlareModerate7.14 Percentage of participants
DUOVISCAqueous Signs - Aqueous FlareSevere0 Percentage of participants
DUOVISCAqueous Signs - Aqueous FlareNone39.29 Percentage of participants
Healon5Aqueous Signs - Aqueous FlareModerate7.69 Percentage of participants
Healon5Aqueous Signs - Aqueous FlareMild65.38 Percentage of participants
Healon5Aqueous Signs - Aqueous FlareSevere0 Percentage of participants
Healon5Aqueous Signs - Aqueous FlareNone26.92 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous FlareSevere0 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous FlareMild53.85 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous FlareNone46.15 Percentage of participants
Amvisc PlusAqueous Signs - Aqueous FlareModerate0 Percentage of participants
Secondary

Aqueous Signs - Corneal Edema

Measured as the percentage of patient's eyes subjectively evaluated to have corneal edema at each of the following gradings: 0 - none; 1 - Mild, slight localized or generalized edema; 2 - Moderate, significant localized or generalized edema; 3 - Severe, advanced localized or generalized edema.

Time frame: 1 day after surgery

Population: This data was collected for all subjects attending the visit one day after surgery.

ArmMeasureGroupValue (NUMBER)
DISCOVISCAqueous Signs - Corneal EdemaNone68.97 Percentage of Participants
DISCOVISCAqueous Signs - Corneal EdemaMild57.59 Percentage of Participants
DISCOVISCAqueous Signs - Corneal EdemaModerate3.45 Percentage of Participants
DISCOVISCAqueous Signs - Corneal EdemaSevere0 Percentage of Participants
DUOVISCAqueous Signs - Corneal EdemaMild21.43 Percentage of Participants
DUOVISCAqueous Signs - Corneal EdemaModerate3.57 Percentage of Participants
DUOVISCAqueous Signs - Corneal EdemaSevere0 Percentage of Participants
DUOVISCAqueous Signs - Corneal EdemaNone75 Percentage of Participants
Healon5Aqueous Signs - Corneal EdemaModerate7.69 Percentage of Participants
Healon5Aqueous Signs - Corneal EdemaMild34.62 Percentage of Participants
Healon5Aqueous Signs - Corneal EdemaSevere0 Percentage of Participants
Healon5Aqueous Signs - Corneal EdemaNone57.69 Percentage of Participants
Amvisc PlusAqueous Signs - Corneal EdemaSevere0 Percentage of Participants
Amvisc PlusAqueous Signs - Corneal EdemaMild34.62 Percentage of Participants
Amvisc PlusAqueous Signs - Corneal EdemaNone65.38 Percentage of Participants
Amvisc PlusAqueous Signs - Corneal EdemaModerate0 Percentage of Participants
Secondary

Intraocular Pressure (IOP)

Measure of intraocular pressure of a patient's eye via tonometry one day after surgery. Measured in mmHg. Normal intraocular pressure is between 10 mmHg and 20 mmHg.

Time frame: 1 day after surgery

Population: This data was collected on all subjects attending the visit one day after surgery with the exception of 3 DisCoVisc subjects, 4 DuoVisc subjects, 2 Healon5 subjects, and 1 AmVisc Plus subject.

ArmMeasureValue (MEAN)Dispersion
DISCOVISCIntraocular Pressure (IOP)21.58 mmHgStandard Deviation 8.42
DUOVISCIntraocular Pressure (IOP)19.48 mmHgStandard Deviation 4.6
Healon5Intraocular Pressure (IOP)20.72 mmHgStandard Deviation 6.61
Amvisc PlusIntraocular Pressure (IOP)18.65 mmHgStandard Deviation 5.56
Secondary

Percent Gain in Corneal Thickness.

Percent Gain in Corneal Thickness between the assessment performed before surgery to that performed after surgery. This was assessed at both the 1 week and 1 month visit. Corneal thickness is measured in micrometers and is evaluated by Pachymetry. A negative number indicates a decrease in corneal thickness.

Time frame: 1 week and month after surgery

Population: Participants analyzed for Baseline to 1 week: 29 DisCovisc, 28 DuoVisc, 26 Healon5, 26 Amvisc Plus.

ArmMeasureGroupValue (MEAN)Dispersion
DISCOVISCPercent Gain in Corneal Thickness.Before Surgery to 1 Week after Surgery2.89 Percent GainStandard Deviation 16.45
DISCOVISCPercent Gain in Corneal Thickness.Before Surgery to 1 Month after Surgery-0.55 Percent GainStandard Deviation 11.79
DUOVISCPercent Gain in Corneal Thickness.Before Surgery to 1 Month after Surgery-1.06 Percent GainStandard Deviation 25.38
DUOVISCPercent Gain in Corneal Thickness.Before Surgery to 1 Week after Surgery7.02 Percent GainStandard Deviation 12.06
Healon5Percent Gain in Corneal Thickness.Before Surgery to 1 Week after Surgery9.92 Percent GainStandard Deviation 15.29
Healon5Percent Gain in Corneal Thickness.Before Surgery to 1 Month after Surgery1.98 Percent GainStandard Deviation 10.57
Amvisc PlusPercent Gain in Corneal Thickness.Before Surgery to 1 Week after Surgery5.06 Percent GainStandard Deviation 12.07
Amvisc PlusPercent Gain in Corneal Thickness.Before Surgery to 1 Month after Surgery-9.11 Percent GainStandard Deviation 22.85
Secondary

Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) Insertion

Surgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during intraocular lens (IOL) insertion. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.

Time frame: Time of Surgery

Population: This data was collected on all subjects undergoing surgery with the exception of 1 DuoVisc subject.

ArmMeasureGroupValue (NUMBER)
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionWorking Space Adequate0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionShallow0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFlat0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFull Chamber Maintenance100 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionShallow0 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFlat0 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionWorking Space Adequate7.14 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFull Chamber Maintenance92.86 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFlat0 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionWorking Space Adequate25.93 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionShallow40.74 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFull Chamber Maintenance33.33 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionShallow7.41 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionWorking Space Adequate44.44 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFull Chamber Maintenance48.15 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During Intraocular Lens (IOL) InsertionFlat0 Percentage of participants
Secondary

Surgeon Surgey - Anterior Dome Maintenance During Phacoemulsification

Surgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during phacoemulsification. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.

Time frame: Time of Surgery

Population: This data was collected on all subjects undergoing surgery with the exception of 1 DuoVisc subject.

ArmMeasureGroupValue (NUMBER)
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFlat0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationShallow0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationWorking Space Adequate0 Percentage of participants
DISCOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFull Chamber Maintenance100 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationShallow0 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationWorking Space Adequate3.57 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFull Chamber Maintenance96.43 Percentage of participants
DUOVISCSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFlat0 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationWorking Space Adequate51.85 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationShallow11.11 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFull Chamber Maintenance37.04 Percentage of participants
Healon5Surgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFlat0 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFull Chamber Maintenance48.15 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationShallow3.7 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationFlat0 Percentage of participants
Amvisc PlusSurgeon Surgey - Anterior Dome Maintenance During PhacoemulsificationWorking Space Adequate48.15 Percentage of participants
Secondary

Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior Capsulotomy

Surgeon reporting of Anterior Chamber Dome Maintenance of a subject's eye during anterior capsulotomy. Evaluated on a subjective scale and reported as percent by response. The following scale is used, from worst to best: Flat, Shallow, Working Space Adequate, Full Chamber Maintenance.

Time frame: Time of surgery

Population: This data was collected on all subjects undergoing surgery with the exception of 1 DuoVisc subject.

ArmMeasureGroupValue (NUMBER)
DISCOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFlat0 Percentage of participants
DISCOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyShallow3.45 Percentage of participants
DISCOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyWorking Space Adequate0 Percentage of participants
DISCOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFull Chamber Maintenance96.55 Percentage of participants
DUOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyShallow3.57 Percentage of participants
DUOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyWorking Space Adequate7.14 Percentage of participants
DUOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFull Chamber Maintenance89.29 Percentage of participants
DUOVISCSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFlat0 Percentage of participants
Healon5Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyWorking Space Adequate48.15 Percentage of participants
Healon5Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyShallow22.22 Percentage of participants
Healon5Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFull Chamber Maintenance29.63 Percentage of participants
Healon5Surgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFlat0 Percentage of participants
Amvisc PlusSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFull Chamber Maintenance25.93 Percentage of participants
Amvisc PlusSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyShallow18.52 Percentage of participants
Amvisc PlusSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyFlat0 Percentage of participants
Amvisc PlusSurgeon Survey - Anterior Chamber Dome Maintenance During Anterior CapsulotomyWorking Space Adequate55.56 Percentage of participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026