Ovarian Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women between 18 and 40 years of age
- People who have been diagnosed with polycystic ovary syndrome (PCOS) based on specific diagnostic criteria (known as the modified Rotterdam criteria), meaning a doctor has confirmed at least 2 of the following 3 features: irregular or absent ovulation, higher-than-normal male hormone levels, or a specific appearance of the ovaries on ultrasound
- People whose doctor has recommended IVF (in vitro fertilization) because of PCOS alone, or PCOS combined with other fertility-related factors such as blocked fallopian tubes or previous unsuccessful fertility treatment (IUI)
- People who have been assessed as suitable for ovarian stimulation as part of IVF treatment
- People whose husband or partner has either normal sperm results, or mildly to moderately reduced sperm quality or quantity
- People who are willing and able to sign a consent form and follow the study procedures throughout the trial
Who may not be able to join:
- People who have structural problems with the uterus that could affect pregnancy, such as uterine shape abnormalities present from birth, large fibroids that change the shape of the uterine cavity, adenomyosis, or other significant uterine conditions
- People who have had major surgery on the ovaries or uterus that may have affected ovarian function or uterine structure — for example, surgery to remove ovarian cysts, endometriosis surgery, fibroid removal, or removal of one ovary
- People who have had 3 or more miscarriages
- People, or their partner, who have a known chromosomal (genetic) abnormality
- People who would be unable to follow the trial schedule or attend required follow-up appointments
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Phuong Duy Nguyen, MD, MS, Hanoi General Hospital
Phone: +84 986656835
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Ongoing pregnancy rate at 12 weeks
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.