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Clinical trial

Investigation of Pathogenic Variants in DNA Repair and Meiotic Genes Associated With Ovarian Reserve and Folliculogenesis in Idiopathic Premature Ovarian Insufficiency Using Whole Exome Sequencing: A Case-Control Study

NCT07587853 is registered in ClinicalTrials.gov with Abdurrahman Hamdi İnan as lead sponsor.

NCT NCT07587853
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Registry record

As filed in ClinicalTrials.gov.

Title
Investigation of Pathogenic Variants in DNA Repair and Meiotic Genes Associated With Ovarian Reserve and Folliculogenesis in Idiopathic Premature Ovarian Insufficiency Using Whole Exome Sequencing: A Case-Control Study
Lead sponsor
Abdurrahman Hamdi İnan
Phase
Observational
Overall status
Not yet recruiting
Start date
June 10, 2026
Completion date
June 10, 2028
Enrollment
100 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

premature ovarian insufficiency