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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06290921
Other study ID # 3472
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date February 22, 2024
Est. completion date February 20, 2025

Study information

Verified date February 2024
Source Clinique Ovo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 400
Est. completion date February 20, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers
Gender Female
Age group 18 Years to 42 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Ovulation triggering
Ovulation triggering when women only 2 dominant follicles as opposed to the clinic's standard of 3 follicles or more

Locations

Country Name City State
Canada Clinique Ovo Montréal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Clinique Ovo

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical Pregnancy Rate clinical pregnancy is the presence of fetal heartbeat at the viability ultrasound 6 to 8 weeks after Frozen Embryo Transfer
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