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Molecular mechanisms behind presumed reduced ovarian reserve and embryo competence in BRCA1/2-mutation carriers in IVF/PGD

Withdrawn
Conditions
ovarian reserve
reduced oocyte availability
10083624
10006291
10033283
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Withdrawn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
Inclusion Criteria

- 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

Exclusion Criteria

- 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
NameTimeMethod
<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
NameTimeMethod
<p>NA</p><br>
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