Genotype-phenotype association study in patients with genetic obesity

Genotype-phenotype association study in patients with genetic obesity - PhaeGAdi

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00034523

Enrollment

Registered

2024-06-26

Start date

2021-10-01

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

E66.8

Interventions

Group 1: For basic testing, only: Human genetics Meal test Ergometry (if the child is old enough) Infection (family) anamnesis Only for the basic examination, if medically indicated: Internal genital

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with monogenic obesity Patients with syndromic obesity Patients with extreme early childhood obesity or adolescents with extreme obesity and suspected new, previously unknown form of genetic obesity

Exclusion criteria

Exclusion criteria: Inability to give consent, e.g. due to lack of German language skills

Design outcomes

Primary

Measure	Time frame
Phenotyping of patients with genetic obesity based on the nature and expression of their clinical features. For this purpose the frequencies of the analysed clinical features are determined and evaluated based on the genetic variant of the patient analysed.	—

Countries

Germany

Contacts

Public ContactMartin Wabitsch

Universitätsklinikum Ulm - Sektion Pädiatrische Endokrinologie und Diabetologie

pedu.sekretariat@uniklinik-ulm.de+4973150057401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026