Assessment of Safety and Efficacy of Gabapentin After Surface Ablation, a Case Control Experimental Study

PHASE1RecruitingINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

December 1, 2024

Primary Completion Date

May 10, 2025

Study Completion Date

June 30, 2025

Conditions
Pain After Photorefractive KeratectomyVAS Will be Used to Assess Pain Postoperative
Interventions
DRUG

Giving post photorefractive keratectomy for pain relief

We plan to conduct a randomized prospective study to assess the efficacy and safety of oral Gabapentin versus oral Diclofenac Potassium for postoperative analgesia in adults undergoing surface ablation. The first group will be given gabapentin orally in a dose of 300mg Tid for 72 hours and the second group will be given oral diclofenac potassium 50mg Tid for 72 hours. The drugs will be administered starting from the first day postoperative.

Trial Locations (1)

Unknown

RECRUITING

Research Institute of Ophthalmolgy, Giza

All Listed Sponsors
lead

Research Institute of Ophthalmology, Egypt

OTHER