Skip to main content
Clinical Trials/NCT06393855
NCT06393855
Recruiting
Not Applicable

Base Curves of Bandage Contact Lenses and Their Effects on Post Transepithelial Photorefractive Keratectomy (Trans-PRK) Vision and Pain: A Prospective Randomized Clinical Trial

Dongyang People's Hospital1 site in 1 country36 target enrollmentJune 18, 2024
ConditionsMyopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myopia
Sponsor
Dongyang People's Hospital
Enrollment
36
Locations
1
Primary Endpoint
Early postoperative uncorrected visual acuity
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The objective of this study was to investigate the impact of employing bandage contact lenses with a base curve of 8.4 mm versus 8.8 mm on visual recovery following Trans-PRK in patients characterized by steep corneas and high myopia.

Detailed Description

Comparing two kind of bandage lenses in the contralateral eyes of the same individual following Trans-PRK may enable the derivation of reliable conclusions regarding the optimal choice for bandage lenses after Trans-PRK.

Registry
clinicaltrials.gov
Start Date
June 18, 2024
End Date
December 31, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Dongyang People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Gengmin Tong

Doctor

Dongyang People's Hospital

Eligibility Criteria

Inclusion Criteria

  • Spherical equivalent refractive error between -6.00 and -8.00 D in either eye.
  • Astigmatism of no more than 2.0 D in either eye.
  • Best spectacle-corrected visual acuity (BCVA) according to the logarithm of the Minimum angle of resolution (logMAR) scale of 0 or better in both eyes.
  • Willing and able to participate in all required activities of the study.

Exclusion Criteria

  • Diabetes mellitus.
  • Systemic connective tissue disease.
  • Cardiovascular disease, epilepsy.
  • Eyelid abnormalities.
  • Corneal disease.
  • A history of ocular disease.
  • Noncompliance with measurement at enrollment.

Outcomes

Primary Outcomes

Early postoperative uncorrected visual acuity

Time Frame: 14 days

All visual acuity measurements were performed using a standard logarithmic eye chart

Secondary Outcomes

  • postoperative pain score after Trans-PRK(2 weeks)
  • re-epithelialization after Trans-PRK(1 week)
  • spherical equivalent after Trans-PRK(1 week)

Study Sites (1)

Loading locations...

Similar Trials