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UnknownNCT02690870

Tamoxifen and Clomiphene Citrate in Mild Stimulation IVF

Comparison of Tamoxifen and Clomiphene Citrate in Mild Stimulation IVF: a Prospective Cohort Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
210 (estimated)
Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Academic / Other
Sex
Female
Age
37 Years – 42 Years
Healthy volunteers
Not accepted

Summary

The purpose of this prospective cohort study is to compare IVF outcome between tamoxifen and clomiphene citrate in mild stimulation.

Detailed description

The reported prevalence of poor ovarian responders amongst patients undergoing IVF-ET is 9%-24%, and morbidity must be higher nowadays. For these women, Mild stimulation has been an important ovulation induction protocol. Clomiphene citrate(CC) and tamoxifen(TMX) are commonly used in mild stimulation protocol. It's reported that CC has adverse effect on growth of endrometrium and results in thin endrometrium(≤7mm) which maybe affect pregnancy rate. However, TMX has estrogen-like effect on the endrometrium that may be helpful to increase endormetrial thickness. The reported results about comparing CC with TMX showed that they had similar ovulation rate. Prospective study is necessary to confirm whether TMX is superior to CC on the IVF outcome.

Conditions

Interventions

TypeNameDescription
DRUGTamoxifenPatients in the tamoxifen group will take 20 mg of tamoxifen oral tablets daily from day 3 of the menses for 5 days.
DRUGClomiphenePatients in clomiphene group will take 100 mg of CC oral tablets daily from day 3 of the menses for 5 days.

Timeline

Start date
2017-01-01
Primary completion
2018-05-01
Completion
2019-03-01
First posted
2016-02-24
Last updated
2016-02-25

Source: ClinicalTrials.gov record NCT02690870. Inclusion in this directory is not an endorsement.