Molecular Genetic Study of Mayer-Rokitansky-Kuster-Hauser Syndrome

Recruiting

• Conditions: Mayer Rokitansky Kuster Hauser Syndrome
• Interventions: Genetic: Biological samples for patients; Genetic: Biological samples for healthy relatives

• Registration Number: NCT02967822
• Lead Sponsor: Imagine Institute

Brief Summary

In order to understand the molecular mechanisms leading to Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH), the research team has to identify molecular bases of this anomaly.

Toward this goal, the research team would like to include in the study patients with MRKH syndrome, as well as their healthy relatives, in order to perform genetic analyses, especially whole exome sequencing.

This study has been set up in order to collect biological samples from patients with MRKH and their relatives.

Detailed Description

The MRKH is a congenital and rare malformation characterised by the absence of the uterus and of 2/3 of the vagina. The incidence is 1 in 4500 female children (46,XX) and a genetic component has been identified.

In order to understand the molecular mechanisms leading to this disease, the research team has to identify the genetic abnormalities.

This study will be led by the research team of the Imagine Institute and the clinical teams associated with the Reference Center for Rare Diseases PGR (Rare Gynecologic Diseases). Both groups are based on the Necker Hospital campus, and already closely collaborate on research into MRKH syndrome.

This collaboration will allow to :

i) collect biological samples from the propositus and their relatives,

ii) have a medical expertise.

The clinicians involved in the study will recruit patients, whose participation will involve providing a biological sample, ie, a blood sample and/or uterine tissue collected during surgical ablation, in the event that surgery is performed during clinical follow-up of the patients. No specific intervention will be planned for the purposes of this study.

In order to perform genetic analysis on trios, the healthy relatives of the patients (parents, brothers, sisters) will also be included. Blood samples will be taken once for healthy relatives.

Genetic analysis, especially whole exome sequencing, will be performed on blood samples by the research team of Imagine Institute.

Study Timeline

• Study Start: 2016-05
• Study First Submitted: 2016-11-14
• Study First Submitted QC: 2016-11-17
• Study First Posted: 2016-11-18
• Status Verified: 2018-10
• Last Update Submitted: 2018-10-10
• Last Update Posted: 2018-10-12
• Primary Completion: 2031-05
• Study Completion: 2031-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 410

Inclusion Criteria

• Patient with MRKH syndrome OR healthy relative of patient included
• Having signed the Informed consent form (or parents in case of patient under 18 years)

Exclusion Criteria

• Refusal to participate in genetic analyses
• Participation in a therapeutical clinical study in the 30 days prior to inclusion in the present study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Patients with MRKH syndrome	Biological samples for patients	Biological samples for patients. Inclusion of patients presenting MRKH syndrome, and who are followed in clinical centres participating in the study.
Healthy relatives	Biological samples for healthy relatives	Biological samples for healthy relatives. Inclusion of healthy relatives of patients included in the study (parents, brothers, sisters)

Primary Outcome Measures

Name	Time	Method
Number of identified nucleotidic variation(s) whose consequences can explain the phenotype of MRKH syndrome	15 years	Genetic cause identification

Trial Locations

Locations (2)

Necker - Enfants malades hospital; 🇫🇷 Paris, France

Institut Mutualiste Montsouris; 🇫🇷 Paris, France