drugset / Trial / NCT06752486

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

NCT06752486

Phase 1 Recruiting 64 enrolled Research Institute of Ophthalmology, Egypt
RandomizedParallel-groupOpen-labelTreatment

Summary

The current study aims at assessing the efficacy and safety of oral Gabapentin alone versus Diclofenac Potassium drugs for postoperative analgesia in patients undergoing surface ablation.

Timeline

Start
2024-12-01
Primary completion
2025-05-10
Completion
2025-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Diclofenac Other / unclassified 50 mg Oral
Comparator Gabapentin Small molecule 300 mg Oral

Indications

No indication recorded.