Clinical Trials Logo

Clinical Trial Summary

WHAT WAS KNOWN

*Standard CXL is the common procedure for treating progressive corneal ectasia. Modifications of the standard protocol were introduces to reduce its complications especially long exposure to ultraviolet rays. The Accelerated protocol, while believed to overcome this issue with comparable outcomes, has not been studied fully in patients with ectasia following corneal refractive surgery and penetrating keratoplasty.

WHAT THIS PAPER ADDS Accelerated CXL is as safe and effective as the Standard CXL in halting the progression of ectasia post refractive surgery and penetrating keratoplasty with the benefit of: reduced ultraviolet exposure, reduced operation time, and reduced patient discomfort.


Clinical Trial Description

Purpose:

The aim of this study is to compare the clinical outcomes of the Standard CXL and the AC CXL in patients with progressive corneal ectasia post refractive surgery and penetrating keratoplasty.

Setting:

Menoufia University Hospital, Egypt

Design:

Prospective, randomised comparison.

Methods:

Patients scheduled to receive either Standard CXL (3mW/cm2 for a period of 30 min) or Accelerated CXL (18mW/cm2 for a period of 5 min).The main outcomes for comparison were the change in; Maximum-K reading (K-max), manifest refractive spherical equivalent (SE), central corneal thickness (CCT), and the best corrected distance visual acuity (CDVA). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03791684
Study type Interventional
Source Menoufia University
Contact
Status Completed
Phase N/A
Start date January 16, 2016
Completion date June 26, 2017

See also
  Status Clinical Trial Phase
Completed NCT00565695 - Evaluation of the Aspheric ReSTOR Intraocular Lens (IOL) After Routine Cataract Extraction N/A
Completed NCT05406973 - Comparison Between the SBK Microkeratome Versus Femtosecond Laser in Flap Creation During LASIK Surgery for Myopia N/A
Active, not recruiting NCT05658718 - Factors Influencing Nocturnal Symptoms After Refractive Surgery.
Recruiting NCT06448468 - Analysis of Ocular Surface Microbiota in Dry Eye Patients After Refractive Surgery
Withdrawn NCT00466908 - Accuracy of the Pentacam and IOL Master to Calculate the Effective Corneal Power After Corneal Refractive Surgery
Completed NCT05060094 - Comparison of Outcomes Between TransPRK and Off-flap Epi-LASIK
Completed NCT04396990 - The RESTORE Study, A Randomized, Controlled, Masked (Reading Center) Prospective Study
Completed NCT03938883 - Ocular Bandage Gel (OBG) Pivotal Trial in Patients Undergoing Photorefractive Keratectomy ("PRK") N/A
Recruiting NCT04281862 - DEXTENZA Compared to Topical Prednisolone in Patients Undergoing Bilateral LASIK Surgery Phase 4
Completed NCT04684888 - Femto-flap Versus SBK Flap,Predictability and Variability N/A
Recruiting NCT06264804 - Risk Factors for Progressive Suction Loss in Corneal Refractive Surgery
Completed NCT03569423 - Comparison Between TPRK Versus AAPRK in Correction of Myopia N/A
Recruiting NCT02614625 - Spectral-domain Optical Coherence Tomography of the Eye N/A
Completed NCT04899258 - Evaluation of the Effect of Myopic Femtosecond Laser Assisted-LASIK on Anterior Chamber Flare Values and Corneal Endothelial Cells: A Prospective Before-and-After Study N/A
Completed NCT00742950 - Refractive Change Induced by 2.8-mm Corneal Incision N/A
Completed NCT03597906 - Topography Guided LASIK by Different Protocols for Treatment of Astigmatism N/A
Recruiting NCT05037370 - CONTOURA vs WFO Ablation PRK & LASIK N/A