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RECRUITING
NCT03059043
NA

Safety and Efficacy Study of A Viscoelastic-free Method for Implantable Collamer Lens (ICL) Implantation

Sponsor: Wenzhou Medical University

View on ClinicalTrials.gov

Summary

This study evaluates the safety and efficacy of a viscoelastic-free method for Implantable Collamer Lens(ICL) implantation to treat high myopia. The subjects undergo randomization of ICL implantation using the viscoelastic-free method on one eye and undergoing standard method on the other one. The post-operative data are collected for analysis.

Official title: Prospective, Multicenter,Randomized Clinical Investigation of A Viscoelastic-free Method for Implantable Collamer Lens (ICL) Implantation to Treat High Myopia: A Pilot Study

Key Details

Gender

All

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2018-11-16

Completion Date

2026-06-22

Last Updated

2024-07-23

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

viscoelastic-free implantation system

Viscoelastic-free implantation system use balanced salt solution irrigation during the implantation

DEVICE

standard viscoelastic-assisted Implantation system

This method utilize the viscoelastic agent to fill and maintain the anterior chamber during the implantation

Locations (5)

Guangdong General Hospital

Guangzhou, Guangdong, China

Hunan Provincial People's Hospital

Changsha, Hunan, China

The Eye Hispital of Wenzhou Medical University

Wenzhou, Zhejiang, China

Peking Union Medical College Hospital

Beijing, China

Shanghai Ninth People's Hospital

Shanghai, China