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Study identifier: NCT06766604 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Super-GDF9 on CAPA-IVM of COCs From Small Antral Follicles

Condition: In Vitro Fertilization  ·  Sponsor: Mỹ Đức Hospital

PhaseNA
Planned participants9
Who can joinFemale, 18 Years to 38 Years
Healthy volunteersNo

About this study

CAPA-IVM (In Vitro Maturation) technology is an assisted reproductive method offering significant benefits in terms of safety and treatment costs, particularly for high-risk patients. These include individuals with ovarian hyperstimulation syndrome (OHSS), venous thrombosis, ovarian torsion, or polycystic ovary syndrome (PCOS). However, while the live birth rate in the CAPA-IVM group (35.2%) is comparable to conventional IVF (43.2%), the number of good-quality embryos and cumulative clinical pregnancy rates remain lower. Improving the CAPA-IVM culture process, particularly through the addition of growth factors found in follicular fluid, has shown promise in enhancing oocyte quality. Growth differentiation factor 9 (GDF9) and Bone morphogenetic protein 15 (BMP15) play critical roles in follicular development, with their heterodimer structure demonstrating the most positive effects on cumulus-oocyte complexes (COCs). Recent studies have identified a potent variant, super GDF9, which is \>1000 times more effective than GDF9 and surpasses cumulin, a heterodimeric growth factor. Super GDF9 enhances cumulus cell expansion and oocyte developmental competence, closely mimicking in vivo maturation. This study investigates the impact of supplementing super GDF9 during CAPA-IVM culture, aiming to improve outcomes of cumulus-oocyte complexes (COCs) from small follicles and ultimately enhance treatment success.

This description comes directly from the study's public registry record.

Talk to the study team

Kha T Huynh  ·  +84946699470  ·  kha.ht@myduchospital.vn

Always discuss trial participation with your own doctor first.

Locations (1)

My Duc HospitalHo Chi Minh City, VietnamRecruiting

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Source record: clinicaltrials.gov/study/NCT06766604