Clinical Trials Directory

Trials / Completed

CompletedNCT06944132

CsA vs MMC for Preventing Pterygium Recurrence

Adjunctive Use of Topical Cyclosporin A Versus Mitomycin C to Prevent Pterygium Recurrence

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Benha University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

aimed to compare the efficacy and safety of topical cyclosporin A (CsA) versus mitomycin C (MMC) as adjunctive therapies in preventing pterygium recurrence after surgical excision.

Detailed description

A total of 40 eyes from 40 patients undergoing pterygium surgery were randomized into two groups: Group A received topical cyclosporin A, while Group B was treated with topical mitomycin C. Ocular surface inflammation scores, recurrence rates, patient-reported symptoms, and adverse effects were assessed at baseline and during follow-up at 6 months postoperatively.

Conditions

Interventions

TypeNameDescription
PROCEDUREExcision of the pterygiumThe surgical procedure involved excision of the pterygium, including the fibrovascular head and associated conjunctival tissue, followed by bare sclera closure using an autologous conjunctival graft harvested from the superior bulbar conjunctiva. The graft was secured in place using either fibrin glue or 8-0 absorbable sutures. In Group B, 0.02% mitomycin C (MMC) was applied to the bare sclera for two minutes using a soaked sponge, followed by thorough irrigation with balanced salt solution.
DRUGPost-operative application of CsAPatients received topical cyclosporin A (0.05%) twice daily for three months postoperatively.
DRUGIntra-operative application of MMC0.02% mitomycin C (MMC) was applied to the bare sclera for two minutes using a soaked sponge, followed by thorough irrigation with balanced salt solution.

Timeline

Start date
2024-04-01
Primary completion
2024-09-30
Completion
2024-10-15
First posted
2025-04-25
Last updated
2025-04-25

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06944132. Inclusion in this directory is not an endorsement.