Molecular mechanisms behind presumed reduced ovarian reserve and embryo competence in BRCA1/2-mutation carriers in IVF/PGD
- Conditions
- ovarian reservereduced oocyte availability100836241000629110033283
- Registration Number
- NL-OMON38833
- Lead Sponsor
- Medisch Universitair Ziekenhuis Maastricht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 245
- IVF/PGD treatment for a BRCA1/2 mutation, both female and male mutation carriers
- IVF/PGD treatment because of an autosomal dominant genetic disorder transmitted by the male
- IVF treatment, including ICSI, for male subfertility
- Previous diagnosis of female subfertility in controls
- Known hereditary disease other than due to BRCA1/2-mutations in the female
- Known history of a malignancy in the female
- History of cancer treatment in the female
- Non-Dutch couples, not able to understand the patient information to give
informed consent properly
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>a) determine the presence of apoptosis, DNA damage, impaired spindle formation<br /><br>or other cell division defects present in the studied biological samples<br /><br>compared to controls. b) exploration and identification of the molecular<br /><br>pathways associated with reduced ovarian reserve and oocyte/embryo competence<br /><br>in BRCA1/2-mutation carriers. </p><br>
- Secondary Outcome Measures
Name Time Method <p>NA</p><br>