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NCT06608186CompletedPhase 1/2

Can Drospirenone be Used to Prevent LH Surge in Controlled Ovarian Stimulation in PCOS?!

Can Drospirenone be Used to Prevent LH Surge in Controlled Ovarian Stimulation in PCOS Cases

Source: ClinicalTrials.gov · Last updated 22 Jan 2025

Brief summary (registry, in English)

The goal of this clinical trial is to learn if drospirenone can work to prevent LH surge in controlled ovarian stimulation in PCOS cases undergoing ART cycles. The main questions it aims to answer are: Can drospirenone prevent LH surge in controlled ovarian stimulation in PCOS cases ? Can it prevent the occurance of ovarian hyperstimulation? Researchers will compare drospirenone to cetrorelix (A well known drug for such cases) to see if drospirenone works the same way. Participants will: Take drospirenone or cetrorelix from stimulation day 5 ( 5 days of ovarian stimulation) till day of hCG trigger \- monitoring will be done before the cycle and through the cycles with vaginal ultrasound assessment and lab testing

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
50 (actual)
First submitted
19 Sept 2024
Start date
1 Oct 2024
Primary completion date
19 Jan 2025
Lead sponsor
Ahmed Saad
NCT number
NCT06608186

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 50
  • From 1 Oct 2024 to the primary completion date, 19 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • previous ovarian surgery

Age

  • age 38 years

Other

  • basal FSH level 12 mIU/mL
  • congenital uterine anomaly anomaly, intrauterine adhesion and male partner with non-obstructive azoospermia.

Who the study is looking for

  • PCOS was diagnosed according to the Rotterdam consensus criteria (two out of three of the following criteria):
    • oligo- or anovulation
    • clinical and/or biochemical signs of hyperandrogenism
    • polycystic ovaries).
  • A diagnosis of congenital adrenal hyperplasia, Cushing's syndrome, androgen-producing tumours, hyperprolactinemia and thyroid dysfunction were all rulled out.

Age in the registry: 20 years to 38 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hawaa Fertility center
Coordinator of this site? Confirm its status
BanhāEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.