Clinical Trials Directory

Trials / Completed

CompletedNCT03830723

Personalized Insemination Treatment Study

Effect of Personalized Dosages of Rekovelle on the Number of Mature Follicles Reached in Intra-uterine Insemination

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Clinique Ovo · Industry
Sex
Female
Age
18 Years – 42 Years
Healthy volunteers
Accepted

Summary

This study is intended for women undergoing their first cycle of 3 intrauterine inseminations. All 3 inseminations will be personalized by using algorithms to determine the dose of study medication.

Detailed description

Study medication dosage for the first insemination cycle will be based on the woman's age as well as her Anti-Mullerian Hormone (AMH) levels. Study medication dosage for the second and third insemination will depend on ovarian response (number of follicles) during previous insemination cycle and woman's age

Conditions

Interventions

TypeNameDescription
DRUGFollitropin deltaStudy medication doses during all 3 insemination will be personalized using a suggested algorithm

Timeline

Start date
2020-01-09
Primary completion
2021-01-20
Completion
2021-09-27
First posted
2019-02-05
Last updated
2022-09-13

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03830723. Inclusion in this directory is not an endorsement.