ClinicalTrials.gg
Not yet recruitingNCT07277426Updated Dec 11, 2025

Comparing Two Surgical Methods to Prevent Pterygium Regrowth

An interventional study of Conjunctival Rotational Flap and Conjunctival Autograft in Pterygium, sponsored by College of Physicians and Surgeons Pakistan. Not yet recruiting. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-12-11.

Sponsored by College of Physicians and Surgeons Pakistan · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 4 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
342
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This study compares two surgical techniques for preventing the regrowth of a pterygium, a non-cancerous growth on the eye. After surgically removing the pterygium, surgeons will cover the area with either a flap of nearby tissue that is rotated into place (Rotational Flap) or with a free graft of tissue taken from under the upper eyelid (Autograft). The main goal is to see which method is better at preventing the pterygium from growing back over a 6-month period. A total of 342 patients with a primary pterygium will be randomly assigned to one of the two surgical groups.

Read the detailed description

This is a single-center, prospective, randomized controlled trial to be conducted at the Department of Ophthalmology, Saidu Group of Teaching Hospital, Swat. The study aims to compare the efficacy of the Conjunctival Rotational Flap versus the Conjunctival Autograft in reducing recurrence rates following primary pterygium excision. Adult patients aged 18-60 with primary pterygium will be enrolled. Participants will be randomly allocated into two groups: Group A (Conjunctival Rotational Flap) and Group B (Conjunctival Autograft). The primary outcome measure is the absence of clinical recurrence, defined as fibrovascular tissue crossing ≥ 1 mm onto the cornea, assessed at the 6-month postoperative follow-up visit via slit-lamp examination. Secondary outcomes may include operative time and postoperative complications. Data will be analyzed using SPSS version 23, with a p-value of ≤ 0.05 considered statistically significant.

02

Conditions studied

  • Pterygium

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Keywords

  • Conjunctival Autograft
  • Conjunctival Rotational Flap
  • Pterygium Recurrence
03

In context

Pterygium

109 studies on the registry are indexed under Pterygium; 9 are open to participants now.

This study's planned enrollment of 342 is above the median of 60 across 93 interventional studies indexed under Pterygium.

Browse Pterygium studies →

Lead sponsor

College of Physicians and Surgeons Pakistan is the lead sponsor of 15 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Age 18-60

      • Either gender
      • Primary pterygium

Exclusion criteria

Exclusion Criteria:

    • Collagen vascular disease

      • disorders
      • Pregnancy
      • Ocular surface infection
      • Previous limbal surgery
      • Recurrent or pseudo-pterygium
      • Ocular trauma
      • Corneal opacity/degeneration'
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
342 participants (estimated)

Study arms

  • Experimental
    Rotational Flap

    A hinged conjunctival flap created adjacent to the excision site and rotated to cover the scleral defect while maintaining partial vascular attachment.

    Procedure: Conjunctival Rotational Flap · Procedure: Conjunctival Autograft

  • Active comparator
    Conjunctival Autograft

    A free conjunctival graft harvested from the superior bulbar conjunctiva and transplanted to the scleral bed after pterygium excision.

    Procedure: Conjunctival Rotational Flap · Procedure: Conjunctival Autograft

Interventions

  • ProcedureConjunctival Rotational Flap

    A surgical technique where adjacent conjunctival tissue, remaining partially attached, is rotated to cover the exposed sclera after pterygium excision.

  • ProcedureConjunctival Autograft

    A surgical technique where a free graft of conjunctiva is harvested from the superior bulbar conjunctiva and sutured or glued over the scleral defect after pterygium excision

06

What researchers measure

Primary outcomes

  1. Pterygium Recurrence Rate

    Absence of clinical recurrence, defined as a quiet ocular surface with no fibrovascular regrowth ≥ 1 mm onto the cornea, as measured by slit-lamp examination.

    Time frame: 6 months postoperatively

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07277426
Lead sponsor
College of Physicians and Surgeons Pakistan
Responsible party
Faiz ur rahman (Postgraduate Resident, Department of Operative Dentistry, College of Physicians and Surgeons Pakistan) — Principal investigator
First posted
Dec 11, 2025
Start date
Feb 2, 2026 (estimated)
Primary completion
Jul 2, 2026 (estimated)
Completion
Jul 2, 2026 (estimated)
Last update
Dec 11, 2025

Study contacts

Muhammad Iqbal, MBBS
Contact
Miqbalskt@gmail.com
+923049208484

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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