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Hydroxypropylmethylcellulose 0.3% and Sodium Hyaluronate 0.18% for Ocular Surface Disease in Glaucoma

Effect of Hydroxypropylmethylcellulose 0.3% and Sodium Hyaluronate 0.18% in the Treatment of Ocular Surface Disease in Glaucoma Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01284439
Enrollment
120
Registered
2011-01-27
Start date
2011-01-31
Completion date
2012-02-29
Last updated
2011-01-27

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

Conditions

Ocular Surface Disease, Glaucoma

Brief summary

To study effect of hydroxypropylmethylcellulose 0.3% and sodium hyaluronate 0.18% in the treatment of ocular surface disease in glaucoma patients.

Interventions

TearA: QID to every 2 hous , 1-2 drops per each time , duration 1 month

DRUGsodium hyaluronate

QID to every 2 hous, 1-2 drops per each time, duration 1 month

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* OSDI \> or equal 20 and eye lid inflammation , meibomian gland inflammation,conjunctival injection,follicle at tarsus , positive corneal staining , tear break up time less than 8 seconds , tear volume less than 5.5 mm.

Exclusion criteria

* Age below 18 yo * Active infectious corneal disease * Post penetrating keratoplasty or glaucoma drainage device * Known allergy to medication * Lactation , Pregnant

Design outcomes

Primary

MeasureTime frame
Ocular surface index score1 month

Secondary

MeasureTime frame
Eye lid inflammation, corneal staining score, tear break up time and tear volume1 month

Countries

Thailand

Contacts

Primary ContactAssocProf Pinnita Tanthuvanit
02-4198036

Outcome results

None listed

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