Clinical Trials Directory

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

TypeNameDescription
DRUGCorifollitoropin alfa (CFA)-double pick upIn 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.

Double Pick up in Poor Prognosis Women (NCT03846544) · Clinical Trials Directory