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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03283852
Other study ID # RBR_2016_16
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 21, 2017
Est. completion date February 21, 2027

Study information

Verified date June 2024
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact Amélie YAVCHITZ, MD, PHD
Phone 01 48 03 64 54
Email ayavchitz@for.paris
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Disorders of growth, puberty and sex development can have genetic causes. The exome analysis could detect new mutations responsible for these disorders and the frequency of these mutations in these disorders, their association with other malformations.


Recruitment information / eligibility

Status Recruiting
Enrollment 1100
Est. completion date February 21, 2027
Est. primary completion date February 21, 2027
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - congenital growth hormone deficiency - puberty disorder - gonadal dysgenesis or anorchia - primary ovarian failure - disorder of sex development - subjects related to a patient with one of the above criteria Exclusion Criteria: - environmental or auto-immune cause

Study Design


Intervention

Genetic:
blood sample
search for genetic mutations

Locations

Country Name City State
France Hôpital Fondation A de Rothschild Paris

Sponsors (1)

Lead Sponsor Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary mutation research frequency of genetic mutation baseline
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