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RecruitingNCT07343011Updated Jan 15, 2026

Conjunctival Transpositional Surgery for Primary Pterygium

An interventional study of Conjunctival Transpositional Pterygium Surgery in Pterygium of the Conjunctiva and Cornea, sponsored by Zahedan University of Medical Sciences. Recruiting at 1 site in Iran. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-15.

Sponsored by Zahedan University of Medical Sciences · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Registered 7 months after the study started (first participant enrolled May 2025, registered Jan 2026).
  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Pterygium of the Conjunctiva and Cornea

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03

In context

Corneal Diseases

219 studies on the registry are indexed under Corneal Diseases; 43 are open to participants now.

This study's planned enrollment of 70 is above the median of 40 across 132 interventional studies indexed under Corneal Diseases.

Browse Corneal Diseases studies →

Lead sponsor

Zahedan University of Medical Sciences is the lead sponsor of 15 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
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

  • Adults aged 18 years or older
  • Primary pterygium involving the cornea
  • Ability to provide

Exclusion criteria

Exclusion Criteria:

  • Recurrent pterygium
  • Previous ocular surface surgery
  • Active ocular infection or inflammation
  • Severe ocular surface disease
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.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Pterygium patients

    Procedure: Conjunctival Transpositional Pterygium Surgery

Interventions

  • ProcedureConjunctival Transpositional Pterygium Surgery

    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.

06

What researchers measure

Primary outcomes

  1. Pterygium Recurrence

    Recurrence is defined as fibrovascular regrowth toward the cornea or surgical failure.

    Time frame: 12 months

Secondary outcomes

  1. Visual Acuity

    Change in visual acuity measured in logMAR units.

    Time frame: 12 months

  2. Refractive Astigmatism

    Change in refractive astigmatism measured as cylindrical power in diopters.

    Time frame: 12 months

07

Study locations

1 of 1 sites recruiting
  • Alzahra Eye Hospital, Zahedan University of Medical Sciences
    Zahedan, Sistan and Balochistan, Iran
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

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 Jan 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07343011
Lead sponsor
Zahedan University of Medical Sciences
Responsible party
Mohammed Arish (Associate professor of ophthalmology, Zahedan University of Medical Sciences) — Principal investigator
First posted
Jan 15, 2026
Start date
May 21, 2025
Primary completion
May 1, 2026 (estimated)
Completion
Jan 1, 2027 (estimated)
Last update
Jan 15, 2026

Study contacts

Mohammed Arish, MD, FRCS
Contact
mohammad.erish@zaums.ac.ir
09151419155

Oversight

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

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