Trials / Completed
CompletedNCT03846544
Double Pick up in Poor Prognosis Women
Double Trigger and Ovum Retrieval vs. Conventional Antagonist Ovarian Stimulation Protocol in Poor Prognosis Women Undergoing IVF/ICSI: A Pilot Randomized Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 48 (actual)
- Sponsor
- CRG UZ Brussel · Academic / Other
- Sex
- Female
- Age
- 25 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this randomized pilot study is to compare the efficacy of double oocyte retrieval vs. conventional antagonist ovarian stimulation protocol in poor prognosis patients undergoing in vitro fertilization (IVF) or intra-cytoplasmic sperm injection (ICSI).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Corifollitoropin alfa (CFA)-double pick up | In the study group, 225 IU of recombinant FSH (rFSH) will continue after the first oocyte retrieval (OR). Antagonist administration will be initiated when at least one follicle measuring ≥14 mm will be present in the ultrasound. If one or more follicles ≥17 mm are observed, patients will undergo a second triggering with human chorionic gonadotropin (hCG) 5000 IU and a second OR will be performed. In case of patients with no follicular development following 10 additional days of rFSH post-OR |
Timeline
- Start date
- 2019-10-01
- Primary completion
- 2021-09-15
- Completion
- 2022-10-01
- First posted
- 2019-02-19
- Last updated
- 2024-05-21
- Results posted
- 2024-04-15
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT03846544. Inclusion in this directory is not an endorsement.