Actively Recruiting
Molecular Genetic Study of Mayer-Rokitansky-Kuster-Hauser Syndrome
Led by Imagine Institute · Updated on 2018-10-12
410
Participants Needed
2
Research Sites
782 weeks
Total Duration
On this page
Sponsors
I
Imagine Institute
Lead Sponsor
R
Reference center for rare diseases (Rare Gynecologic Diseases)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Molecular Genetic Study of Mayer-Rokitansky-Kuster-Hauser Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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)
You will not qualify if you...
- Refusal to participate in genetic analyses
- Participation in a therapeutical clinical study in the 30 days prior to inclusion in the present study.
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Necker - Enfants malades hospital
Paris, France, 75015
Actively Recruiting
2
Institut Mutualiste Montsouris
Paris, France
Actively Recruiting
Research Team
S
Stanislas Lyonnet
CONTACT
A
Anna Pelet
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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