Clinical Trials Directory

Trials / Completed

CompletedNCT05737979

Modified Rekovelle and Menopur Combination Protocol to Avoid Monitoring Before Day 10 of Stimulation

Status
Completed
Phase
Study type
Observational
Enrollment
772 (actual)
Sponsor
Clinique Ovo · Industry
Sex
Female
Age
18 Years
Healthy volunteers

Summary

Follitropin delta (Rekovelle) algorithm established by Ferring provides personalized gonadotrophin doses based on each patient's weight and AMH. As a result, risks of stimulation failure or ovarian hyperstimulation syndrome (OHSS) during an in vitro fertilization (IVF) cycle are minimized. As a standard practice for OHSS prevention at clinique ovo, women undergoing IVF will have a scheduled ultrasound and blood test on the sixth day of their stimulation treatment. However, with the determination of the Rekovelle and Menopur algorithm, the risks of OHSS before the tenth day have been considerably minimized.

Detailed description

The purpose of this study is to evaluate the necessity of programming an ultrasound and blood test prior to the tenth day of ovarian stimulation when women are on personalized doses of Rekovelle and Menopur duting an antagonist IVF cycle. Based on the results of the analysis, we will assess the economic impact that programming an ultrasound and blood test at day 10 might have.

Conditions

Interventions

TypeNameDescription
OTHERStudy chart reviewEvaluation of the IVF cycle using the prescribed medication

Timeline

Start date
2023-01-27
Primary completion
2023-11-30
Completion
2024-01-27
First posted
2023-02-21
Last updated
2024-02-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05737979. Inclusion in this directory is not an endorsement.