About this trial
This prospective single-arm interventional study evaluates the recurrence rate and functional outcomes following conjunctival transpositional pterygium surgery without bare sclera formation. The technique involves mobilization and transposition of the pterygium tissue while preserving Tenon's layer and avoiding adjunctive therapies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged 18 years or older
Primary pterygium involving the cornea
Ability to provide informed consent
Disqualifiers
Recurrent pterygium
Previous ocular surface surgery
Active ocular infection or inflammation
Severe ocular surface disease
Trial design
Single group
Treatments tested in this trial
Conjunctival Transpositional Pterygium Surgery
Procedure/SurgeryA conjunctival incision was created at the upper and lower limbus to allow adequate tissue mobilization. The pterygium tissue is dissected off the corneal surface without complete excision or creation of a bare sclera defect. The fibrovascular tissue is mobilized and transposed inferiorly within the subconjunctival plane and secured with absorbable sutures. Tenon's tissue is preserved, and no adjunctive therapy is used.
Treatment groups
Trial outcomes
Primary outcomes
Pterygium Recurrence
Recurrence is defined as fibrovascular regrowth toward the cornea or surgical failure.
Secondary outcomes
Visual Acuity
Change in visual acuity measured in logMAR units.
Refractive Astigmatism
Change in refractive astigmatism measured as cylindrical power in diopters.
Sponsors and contacts
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