Clinical Trials Directory

Trials / Unknown

UnknownNCT02114645

The Effect of GnRH Agonist Administered in the Luteal Phase on ART Cycle Outcomes

To Evaluate the Effect of GnRH Agonist Administered in the Luteal Phase on ART Cycle Outcomes in Both GnRH Agonist and GnRH Antagonist Treated Ovarian Stimulation Protocols

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Zekai Tahir Burak Women's Health Research and Education Hospital · Academic / Other
Sex
Female
Age
18 Years – 38 Years
Healthy volunteers
Accepted

Summary

This prospective clinical trial evaluates the effect of a two dose GnRH agonist administered in the luteal phase on the outcome of ART cycles stimulated with the long GnRH agonist and GnRH antagonist protocol.

Detailed description

This prospective clinical trial evaluates the effect of a two dose GnRH agonist administered in the luteal phase on the outcome of ART cycles stimulated with the long GnRH agonist and GnRH antagonist protocol. Decision between each of these two protocols was subjective and depended on the clinical context.In addition to routine luteal phase support with progesterone and estradiol valerate,women received two dose of GnRH agonist on the fifth and tenth day after ET.Live birth rate was the primary outcome measure.

Conditions

Interventions

TypeNameDescription
DRUGLeuprolide acetatein experimentals groups,on fifth and tenth day after embryo transfer 0,5mg leuprolide acetate is given subcutaneously as luteal phase support
DRUGvaginal progesteronecrinone gel is applied till fetal heart beat is detected
DRUG4 mg oral estradiol valerateestrofem is given twice a day

Timeline

Start date
2014-04-01
Primary completion
2015-02-01
Completion
2015-04-01
First posted
2014-04-15
Last updated
2014-04-15

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02114645. Inclusion in this directory is not an endorsement.