Conjunctival Transpositional Surgery for Primary Pterygium
Conjunctival Transpositional Pterygium Surgery: A Prospective Single-Arm Interventional Study
1 other identifier
interventional
70
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 21, 2025
CompletedFirst Submitted
Initial submission to the registry
January 6, 2026
CompletedFirst Posted
Study publicly available on registry
January 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
ExpectedJanuary 15, 2026
January 1, 2026
12 months
January 6, 2026
January 6, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Pterygium Recurrence
Recurrence is defined as fibrovascular regrowth toward the cornea or surgical failure.
12 months
Secondary Outcomes (2)
Visual Acuity
12 months
Refractive Astigmatism
12 months
Study Arms (1)
Pterygium patients
EXPERIMENTALInterventions
A 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.
Eligibility Criteria
You may qualify if:
- Adults aged 18 years or older
- Primary pterygium involving the cornea
- Ability to provide informed consent
You may not qualify if:
- Recurrent pterygium
- Previous ocular surface surgery
- Active ocular infection or inflammation
- Severe ocular surface disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Alzahra Eye Hospital, Zahedan University of Medical Sciences
Zahedan, Sistan and Balochistan, Iran
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate professor of ophthalmology
Study Record Dates
First Submitted
January 6, 2026
First Posted
January 15, 2026
Study Start
May 21, 2025
Primary Completion
May 1, 2026
Study Completion (Estimated)
January 1, 2027
Last Updated
January 15, 2026
Record last verified: 2026-01