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
| Type | Name | Description |
|---|---|---|
| DRUG | Follitropin delta | Study 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.