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Effect of Superficial Keratotomy on Reducing Postoperative Pain Fallowing Conjuctival Flap.

Effect of Superficial Keratotomy on Reducing Postoperative Pain Fallowing Conjuctival Flap ;a Randomized Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220424054640N2
Enrollment
16
Registered
2022-05-14
Start date
2022-05-21
Completion date
Unknown
Last updated
2022-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe visual impairment, monocular. Severe visual impairment, monocular

Interventions

Intervention 1: Intervention group:we use the modified surgical method, the conj flap operation with cutting the superficial nerves of the cornea. Intervention 2: Control group:we use the classical Gu

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: VLE (vision loss eye) Patients who are candidates for prosthesis implantation

Exclusion criteria

Exclusion criteria: Patients who are candidates for conjunctival flap with indications other than implant placement (such as pain due to corneal ulcers, etc.) painful vision loss eye

Design outcomes

Primary

MeasureTime frame
In the study of the effect of superficial corneal incisions in reducing pain in patients after conjunctival flap surgery, primary outcome can be the pain score after Corneal neurotomy . Timepoint: In the study of the effect of superficial corneal incisions in reducing pain in patients after conjunctival flap surgery, pain score measurement can be 6 24 48 hours after corneal neurotomy. Method of measurement: In studying the effect of superficial corneal incisions in reducing pain in patients after conjunctival flap surgery, how to measure pain score can be using VSA(visual analogue scale ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Nasser Karimi

Iran University of Medical Sciences

drnasserkarimi@gmai.com+98 21 6655 8811

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026