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Enrolling by invitationNCT07198126Updated Sep 30, 2025

Comparison Of Keratometric Readings Pre and Post Pterygium Excision With Conjunctival Autograft Transplantation

An interventional study of Pterygium Excision with Conjunctival Autograft in Pterygium and Corneal Astigmatism, sponsored by Mughal Eye Trust Hospital. Enrolling by invitation at 1 site in Pakistan. Open to participants aged 30 Years to 70 Years. Per ClinicalTrials.gov, last updated 2025-09-30.

Sponsored by Mughal Eye Trust Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Feb 2026, 8 months ago, but the record still lists the study as enrolling by invitation.
Phase
Not applicable
Study type
Interventional
Enrollment
130
Allocation
Not applicable
Ages
30 Years to 70 Years
Sex
All
01

Study summary

Pterygium, often called "surfer's eye," is a common eye condition in which a raised, fleshy growth of tissue extends from the white part of the eye onto the clear cornea. This growth can cause redness, irritation, blurred vision, and, in advanced cases, changes in the curvature of the cornea leading to distorted vision (astigmatism). The condition is more frequent in people exposed to sunlight, dust, and dry environments.

The standard treatment for symptomatic pterygium is surgical removal. However, simple removal has a high chance of recurrence. To reduce this risk, surgeons commonly use a technique called conjunctival autograft transplantation, where a small piece of the patient's own conjunctiva is placed over the area after excision. This method not only lowers the recurrence rate but may also improve vision by reducing corneal irregularities.

This study is designed to measure the changes in corneal curvature (keratometric readings) before and after pterygium excision with conjunctival autograft transplantation. By comparing preoperative and postoperative measurements, the study aims to determine how much this surgery improves corneal shape and reduces astigmatism.

The hypothesis is that pterygium excision with conjunctival autograft transplantation will lead to a significant improvement in keratometric readings and reduce irregular astigmatism, thereby improving visual quality.

This research will provide local evidence of the effectiveness of this procedure and help guide treatment strategies for patients suffering from pterygium-related visual problems.

02

Conditions studied

  • Pterygium
  • Corneal Astigmatism

Keywords

  • Pterygium excision
  • Astigmatism correction
  • Conjunctival autograft transplantation
  • Refractive error
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 130 is above the median of 60 across 93 interventional studies indexed under Pterygium.

Browse Pterygium studies →

Lead sponsor

Mughal Eye Trust Hospital is the lead sponsor of 2 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
30 Years to 70 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

  • Adults of either sex aged >30 to 70 years.
  • Phakic eyes.
  • Primary pterygium, Grade II or Grade III (as per protocol grading).
  • Presence of corneal astigmatism on pre-operative assessment.
  • Scheduled for pterygium excision with conjunctival autograft transplantation at the study site.
  • Able to provide written and to attend the 1-month postoperative assessment.

Exclusion criteria

Exclusion Criteria:

  • Pseudophakic or aphakic eyes.
  • Recurrent pterygium.
  • Prior keratoplasty or trabeculectomy in the study eye.
  • Keratoconus or other corneal pathologies that can independently induce astigmatism.
  • Lenticular astigmatism or significant lens pathology affecting refraction.
  • Eyes planned for simple pterygium excision without conjunctival autograft.
  • Any ocular condition or systemic illness judged likely to interfere with keratometric or refractive measurements, follow-up, or surgical safety.
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
130 participants (estimated)

Study arms

  • Experimental
    Group Pterygium Excision with Conjunctival Autograft

    Patients will undergo surgical excision of pterygium followed by conjunctival autograft transplantation. The autograft will be harvested from the superior bulbar conjunctiva and secured at the excision site using sutures.

    Procedure: Pterygium Excision with Conjunctival Autograft

Interventions

  • ProcedurePterygium Excision with Conjunctival Autograft

    Excision of primary Grade II or Grade III pterygium Conjunctival autograft harvested and transplanted at the excision site Graft secured with sutures

06

What researchers measure

Primary outcomes

  1. Change in Keratometric Readings (K1 and K2)

    Keratometric readings, including the flat meridian (K1) and steep meridian (K2) of the anterior corneal surface, will be measured using a manual keratometer. The mean change in K-readings (measured in diopters) from baseline (pre-operative) to post-operative assessment will be calculated to evaluate corneal curvature improvement following pterygium excision with conjunctival autograft.

    Time frame: Baseline (pre-operative) and 1 month post-operative.

Secondary outcomes

  1. Change in Astigmatism

    Astigmatism will be measured using an automated refractometer. Both type (regular/irregular, with-the-rule/against-the-rule) and degree of astigmatism (in diopters) will be recorded. The reduction in astigmatism from baseline to post-operative follow-up will be assessed.

    Time frame: Baseline (pre-operative) and 1 month post-operative.

07

Study locations

1 site
  • Mughal Eye Hospital Trust
    Lahore, Punjab Province 54000, Pakistan
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2025 (actual). Primary completion is estimated for Feb 2026, 5 months after the start.

Of 18 interventional studies with no phase under Pterygium, half reached primary completion within 17 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 28. This study's planned 5 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 21, 2025
First posted
Sep 30, 2025
StartActual
Aug 30, 2025
Primary completionEst.
Feb 28, 2026
CompletionEst.
Feb 28, 2026
Last update
Sep 30, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07198126
Lead sponsor
Mughal Eye Trust Hospital
Responsible party
Ayeza Nadeem Butt (Principal Investigator, Mughal Eye Trust Hospital) — Principal investigator
First posted
Sep 30, 2025
Start date
Aug 30, 2025
Primary completion
Feb 28, 2026 (estimated)
Completion
Feb 28, 2026 (estimated)
Last update
Sep 30, 2025

Oversight

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

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