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Effectiveness Evaluation of CTR for Cataract Surgeries for Patients with Anterior Hyaloid Membrane Detachment.

Effectiveness Evaluation of CTR for Cataract Surgeries for Patients with Anterior Hyaloid Membrane Detachment.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042200017
Enrollment
90
Registered
2020-06-08
Start date
2020-08-24
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Anterior Hyaloid Membrane Detachment

Interventions

Insertion of Capsular Tension Ring into the lens capsule.

Sponsors

Shibata Teppei
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients who are able to fully understand about the participation in the study and then give a written consent voluntarily and by themselves. 2)Patients who are scheduled for a lens extraction by phacoemulsification 3)Patients whose age is between 65 and 90 years at the time when giving his/her consent. 4)Patients who require a lens power from +6.00 D to 30.0 D in the study eye 5)Patients with expected postoperative CDVA of 0.5 in decimal or higher 6)Patients who are able to cooperate with postoperative follow-up visits 7)Patients with confirmed AHM detachment

Exclusion criteria

Exclusion criteria: 1)Retinal detachment 2)A medical history of vitreous surgery 3)Diabetic retinopathy 4)Macular degeneration 5)Rubeosis iridis 6)Atopic cataract 7)Pseudoexfoliation syndrome 8)Single eye status 9)The density of cornea endothelial cell of 500cells/mm2 or less 10)Glaucoma 11)Active uveitis 12)Any abnormality in corneal epithelium, stroma or endothelium that might influence the visual acuity 13)Scheduled for other intraocular surgery besides the cataract surgery during the study period 14)Strabismus, amblyopia, or congenital ocular abnormalities 15)Psychiatric disorders or any impairment in cognitive functions 16)Judged to be ineligible by investigators for any other reasons such as a general or ophthalmic disease. 17)Anterior capsule incision (continuous curvilinear capsulorrhexis) was performed imperfectly. 18)The capsule was damaged during the surgery. 19)Serious adverse events, such as vitreous prolapse, occurred during the surgery. 20)The investigator judged him/her to be ineligible.

Design outcomes

Primary

MeasureTime frame
Decentration and tilt of Intraocular lens

Secondary

MeasureTime frame
-Presence/absence of posterior capsular folds made from the aspiration-point obstruction -Changes in anterior capsular contraction -Changes in anterior chamber depth -Uncorrected/Corrected distance visual acuity -Subjective/Objective refraction -Adverse events, device deficiencies

Contacts

Public ContactTeppei Shibata

Kanazawa Medical University Hospital

prefse74@kanazawa-med.ac.jp+81-76-286-3511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026