Assessment Of Safety And Efficacy Of Gabapentin For Postoperative Analgesia After Surface Ablation: A Randomized Controlled Trial
Published 2026 - 44th Congress of the ESCRS
Reference: FP27.05 | Type: Free paper | DOI: 10.82333/nftj-kv29
Authors: Prof. Dr Mohamed Tarek Tarek Elnaggar* 1
1Refractive surgery Department,Research Institute of Ophthalmology,Giza,Egypt
Purpose
Postoperative pain remains a significant challenge after advanced surface ablation (ASA) and photorefractive keratectomy (PRK). Gabapentin, with its multimodal analgesic properties, has emerged as a promising option for postoperative pain management.
Objective: To assess the efficacy and safety of oral gabapentin compared to oral diclofenac potassium for postoperative analgesia in patients undergoing surface ablation procedures.
Setting
Refractive surgery Department
Research Institute of Ophthalmology, Giza, Egypt
Methods
This prospective, randomized controlled clinical trial included 58 patients (116 eyes) aged 21–37 years (mean 23 ± 4.62 years). Patients were randomized into two groups: Gabapentin group (n=29, receiving 300 mg three times daily) and Diclofenac group (n=29, receiving 50 mg three times daily) for 7 days postoperatively. Pain intensity was assessed daily using the Numeric Rating Scale (NRS) from day 1 to day 7 post-op.
Results
The Gabapentin group demonstrated significantly lower mean pain scores compared to the Diclofenac group across all postoperative days (Day 1: 6.2 ± 0.9 vs. 7.1 ± 0.8; Day 7: 0.3 ± 0.6 vs. 1.2 ± 0.9; p<0.05). Pain relief was faster and more pronounced in the gabapentin group, with complete pain resolution by day 6–7.
Conclusions
Oral gabapentin provides superior postoperative analgesia compared to
diclofenac following surface ablation procedures, with favorable safety profile