DRKS00034523
Recruiting
Not Applicable
Genotype-phenotype association study in patientswith genetic obesity - PhaeGAdi
niversitätsklinikum Ulm - Sektion Pädiatrische Endokrinologie und Diabetologie0 sites50 target enrollmentJune 26, 2024
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- E66.8
- Sponsor
- niversitätsklinikum Ulm - Sektion Pädiatrische Endokrinologie und Diabetologie
- Enrollment
- 50
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility 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
- •Inability to give consent, e.g. due to lack of German language skills
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Association between genotype and clinical course of amyotrophic lateral sclerosisamyotrophic lateral sclerosisJPRN-UMIN000030729Toranomon Hospital Kajigaya
Completed
Not Applicable
Investigation on associations of genotype and phenotype in patients with DysfibrinogenemiaD68.2Hereditary deficiency of other clotting factorsDRKS00014093Klinikum der Johann Wolfgang Goethe-Universität Frankfurt am Main69
Recruiting
Not Applicable
Genetics and its influence on physical characteristics in Indian Patients with Congenital Adrenal Hyperplasia due to 21-α hydroxylase deficiency.Health Condition 1: E250- Congenital adrenogenital disordersassociated with enzyme deficiencyCTRI/2019/04/018430A
Completed
Not Applicable
Association study of genome for common disease, especially circulatory diseases, renal disases and hypertension.JPRN-UMIN000013004Yokohama City University Graduate School of Medicine1,000
Completed
Not Applicable
Study on genotype and phenotype relation by genome analysis of responsible gene region in SMASpinal Muscular AtrophyJPRN-UMIN000040095Institute of Medical Genetics, Tokyo Women's Medical University50