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Clinical Trials in China / NCT03115710
Recruiting Observational

The K-Map Study, Global Prevalence of KC

NCT03115710 · tracked via the Priya Life Science China tracker
Sponsor
University Hospital, Geneva
Phase
Observational
Started
2015-12-28
Last updated
2025-08-11

Condition(s) studied

Keratoconus

Investigational drug(s) / intervention(s)

Rotating Scheimpflug camera (Pentacam HR)

Rotating Scheimpflug camera (Pentacam HR): One visit to Ophthalmology Department is required from participant. Parents or legal guardians must attend with their child. The interview and test during visit take approximately 15 minutes. Interview includes filling out a questionnaire about risk factors of the disease and double check on understanding the consent form. The child will sit in front of the instrument (Pentacam HR Scheimpflug imaging system). The rotational measuring procedure generates Scheimpflug images in three dimensions. The images taken during the examination are digitalized, and all image data are transferred to the computer. It calculates a 3D virtual model of the anterior eye segment, from which all additional information is derived.

Study summary

Keratoconus is a ocular disease classified under ectatic diseases which often results in bilateral and asymmetrical corneal distortion. It usually affects patients at young age and can cause severe visual loss.

The overall goal of this study is to assess the prevalence of keratoconus (KC) in children and adolescents in various regions of the world based on modern tomographic imaging methods, and to verify whether the occurrence rates reported from literature should be corrected. Our hypothesis is that the prevalence of the disease is much higher than that traditionally reported.

At each site, corneal tomography examinations (Pentacam) will be performed bilaterally in children and adolescents, who are not ill or with any ophthalmological symptom. The population to be studied will be composed of children and adolescents on medical visits for non-ophthalmologic reasons, aged between 6 and 20 years. Multiple cities, from different continents (North America, South America, Asia and Europe) will participate.

Eligibility

Sex
ALL
Min age
6 Years
Max age
23 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Male or female, 6-23 years of age. * Subjects seen for a non-ophthalmic appointment * Provide signed and dated patient consent form (signed by parents / legal guardians). * Willing to comply with all study procedures and be available for the duration of the study Exclusion Criteria: * Patients with a preexisting ocular disease / condition * Pregnancy or breastfeeding

Primary outcome measure(s)

Trial sites (12)

FacilityCityRegionStatus
USC Roski Eye Institute Los Angeles California Recruiting
Eye Hospital of Wenzhou Medical College Wenzhou China Recruiting
Zagreb Croatia Recruiting
Alexandria Egypt Recruiting
Homburg Germany Recruiting
Isfahan Iran Recruiting
Amman Jordan Recruiting
Monterrey Mexico Recruiting
Lima Peru Recruiting
Ufa Eye Research Intitute Ufa Russia Completed
King Saud University Riyadh Saudi Arabia Completed
Bukhara Uzbekistan Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03115710 on ClinicalTrials.gov ↗ ← All trials in China