- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06290921
Ovulation Triggering 2 Vs 3 Follicles
March 17, 2025 updated by: Clinique Ovo
Ovulation Trigger with Less Than 3 Follicles in Stimulated In-vitro Fertilization (IVF) Cycles
Poor responders in in-vitro fertilization (IVF) cycles represent a major challenge for fertility specialists.
Although poor responders tend to have sub-optimal fertility treatment outcomes, many of these patients wish to attempt at least one IVF cycle.
Traditionally, IVF cycles producing less than 3 to 4 mature follicles (measuring at least 14 mm) have either been cancelled or converted to intra-uterine insemination (IUI) due to the low pregnancy rates associated with these cycles.
The minimal number of follicles required to proceed with egg collection is based on clinical experience, having been determined by weighing the probability of implantation and pregnancy versus the risk of not obtaining quality oocytes or reaching embryo transfer when fewer mature follicles are present.
This retrospective quality control study aims to compare pregnancy rates in IVF cycles producing 3 follicles measuring 14 mm and more on trigger day, versus 2 or fewer follicles.
Study Overview
Study Type
Observational
Enrollment (Actual)
405
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Quebec
-
Montréal, Quebec, Canada, H4P 2S4
- Clinique ovo
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Data spreadsheet from 2011 to 2017 of patients having undergone an IVF cycle
Description
Inclusion Criteria:
- Stimulated IVF cycle at clinique ovo
- Patients with a maximum of 3 mature follicles (≥14mm) on the day of ovulation trigger
Exclusion Criteria:
- Cycle cancelation due to no follicles
- History of recurrent implantation failure
- Contraindication of ovulation induction medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical Pregnancy Rate
Time Frame: 6 to 8 weeks after Frozen Embryo Transfer
|
clinical pregnancy is the presence of fetal heartbeat at the viability ultrasound
|
6 to 8 weeks after Frozen Embryo Transfer
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Louise Lapensée, MD, Clinique ovo
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 22, 2024
Primary Completion (Actual)
April 1, 2024
Study Completion (Actual)
June 11, 2024
Study Registration Dates
First Submitted
February 26, 2024
First Submitted That Met QC Criteria
February 26, 2024
First Posted (Actual)
March 4, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 17, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3472
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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