Skip to main content
OpenTrials
Completed

NCT Number: NCT03270761

Zhongshan Iridocorneal Endothelial Syndrome Study (ICEs)

This is a multi-center study to report the demographic profile, clinical features, and management in patients with Iridocorneal endothelial (ICE) syndrome in China.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Zhongshan Ophthalmic Center

Guangzhou, Guangdong, 510060, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of ICE syndrome;
  • Those willing to sign the informed consent.

Exclusion criteria

  • Patients who don't sign the informed consent or abide by the study procedure.

Treatment and study plan

Primary outcomes

  1. Management in patients with Iridocorneal endothelial (ICE) syndrome

    Time frame: through study completion, an average of 1 year

    Record the number of medication treating corneal edema or glaucoma, and surgery (anti-glaucoma surgery, keratoplasty)

Secondary outcomes

  1. Demographic profile of patients

    Time frame: 1 day

    Range of age, gender

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Collaborators

  • ICE study group

Registry information

Official study title

A Multi-center Study on Iridocorneal Endothelial (ICE) Syndrome in China

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Sep 1, 2017
Registry last updated
Jun 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.