Clinical Trials Directory

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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

TypeNameDescription
DIAGNOSTIC_TESTPregnancy RateThe 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.