Trials / Unknown
UnknownNCT03684421
Clinical and Live Birth Rates After Following Long Antagonist Protocol Versus Classical Antagonist Protocol
Clinical and Live Birth Rates After Controlled Ovarian Stimulation With the Long Antagonist Protocol Versus Classical Antagonist Protocol
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 120 (estimated)
- Sponsor
- Assisting Nature · Academic / Other
- Sex
- Female
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Accepted
Summary
A randomized prospective study of the evaluation of the clinical IVF results after following Long Antagonist protocol for controlled ovarian stimulation versus following classical antagonist protocol
Detailed description
A randomized prospective study of administration of Degarelix in late luteal phase of women undergoing ovarian stimulation for IVF: Single dose of Degarelix (24mg, 16mg or 12 mg), on day 24th of previous luteal face cycle, was administered. The Clinical Pregnancy and Live Birth Rates were estimated for this group of patients, comparing to the rates of the group which followed classical antagonist protocol. The number of the formed blastocysts in each group is measured, as well.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Pregnancy Rate | The clinical pregnancy and live birth rate according to the protocol of COS |
Timeline
- Start date
- 2017-02-15
- Primary completion
- 2021-06-30
- Completion
- 2021-06-30
- First posted
- 2018-09-25
- Last updated
- 2020-10-08
Locations
1 site across 1 country: Greece
Source: ClinicalTrials.gov record NCT03684421. Inclusion in this directory is not an endorsement.