Renal HYPODYSPLASIA : Genetic and Familial Assessment

Completed

• Conditions: Renal HYPODYSPLASIA, Nonsyndromic, 1

• Registration Number: NCT00925379
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

Evaluation of the frequency of familial cases of renal HYPODYSPLASIA

Detailed Description

DNA collection from the propositus and its family. A questionnaire will be filled by the parents to seek other affected individual in the family.With another affected member, DNA collection will be collected from the whole family.

A renal ultrasound will be prescribed for the parents, brothers and sisters.

Study Timeline

• Study Start: 2009-04
• Study First Submitted: 2009-06-19
• Study First Submitted QC: 2009-06-19
• Study First Posted: 2009-06-22
• Primary Completion: 2013-04
• Status Verified: 2014-07
• Study Completion: 2014-07
• Last Update Submitted: 2014-07-25
• Last Update Posted: 2014-07-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 342

Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluation of the heritability of renal HYPODYSPLASIA (on the renal ultra sound) and DNA collection to make possible identification of predisposing genes	the same day

Trial Locations

Locations (1)

Necker Hospital; 🇫🇷 Paris, France