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

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

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38833
Enrollment
245
Registered
2013-02-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ovarian reserve reduced oocyte availability

Interventions

None listed

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
a) determine the presence of apoptosis, DNA damage, impaired spindle formation or other cell division defects present in the studied biological samples compared to controls. b) exploration and identification of the molecular pathways associated with reduced ovarian reserve and oocyte/embryo competence in BRCA1/2-mutation carriers.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)