RP Cure Tracker

Trials / NCT06239064

Early Genetic Identification of Obesity

Underway, not enrolling Observational Natural history / observational

Sponsor
Rolfs Consulting und Verwaltungs-GmbH (RCV)
Treatment
Genetic testing via blood collection
Gene
Not stated
Conditions
Obesity, Childhood, Hyperphagia, Retinopathy, Syndactyly, Polydactyly, Cognitive Impairment, Bardet-Biedl Syndrome, POMC Deficiency
Ages
2 Years to no upper limit
Enrollment
1000 participants
Started
2024-01-24
Main results expected
2026-03-01
Results posted
Not yet
Record last updated
2025-09-29

What the study is testing

TITLE: Whole genetic approach in Early Genetic Identification of Obesity (WEGIO)

DESIGN: Multicenter epidemiological study

STUDY POPULATION: Participants at risk for a syndromic or a monogenic genetic obesity, incl. participants clinically diagnosed with Bardet-Biedl-Syndrome (BBS)

NUMBER OF PARTICIPANTS: 1000 for initial genetic sequencing and app. 40 for the follow-up documentation

COORDINATING INVESTIGATOR: Prof. Dr. Arndt Rolfs

Where it runs

Germany (37)

Open on ClinicalTrials.gov for contacts and eligibility