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Clinical Trial Summary

The purpose of this study is to compare healing times and subjective pain level responses of nepafenac to placebo after photo refractive keratomileusis (PRK) surgery.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00330798
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase Phase 4
Start date February 2006
Completion date June 2006

See also
  Status Clinical Trial Phase
Completed NCT04704518 - Phase IV Study to Evaluate the Efficacy of Lagricel® Ofteno PF Compared to Thealoz® Duo After Photorefractive Keratectomy (PRK) Phase 4
Completed NCT04281004 - Processed Amniotic Fluid (PAF) Drops After Photorefractive Keratectomy (PRK) Phase 1/Phase 2
Recruiting NCT05313425 - Effect of Ectoine After Photorefractive Keratectomy (PRK).
Recruiting NCT05477875 - Cannabinoid vs Opioid for Photorefractive Keratectomy Pain Control Phase 2
Completed NCT05973253 - Evaluation of Efficacy and Safety of Topical 1% Medroxyprogesterone in the Corneal Epithelium Healing After PRK Phase 2/Phase 3
Terminated NCT01381731 - A Double-masked, Randomized, Placebo-controlled,Pilot Study of Diquafosol Tetrasodium in Subjects Following Photorefractive Keratectomy (PRK) Phase 2