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uteal phase support during frozen embryo transfer cycle

Phase 3
Conditions
Female infertility, unspecified.
Female infertility, unspecified
Registration Number
IRCT201611011141N24
Lead Sponsor
Royan institute, Vice chancellor for research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

Patients with surplus embryos undergone infertility treatment cycles (e.g. OHSS, inadequate endometrium, surplus frozen embryo from any cause); Age 21-37 years; Normal BMI (18.5 Exclusion criteria: Endometrial thickness =7mm; Egg Donors; Surrogacy; Male factor infertility with azoospermia; Age <37 years old; Hydrosalpinx; Uterine anomalies; Myoma with a compression effect or submocusa myoma; PGD; Blastocyst embryo transfer, ZIFT and GIFT.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ongoing pregnancy rate. Timepoint: 6 & 12 weeks of pregnancy. Method of measurement: ultrasonography.
Secondary Outcome Measures
NameTimeMethod
Estrogen. Timepoint: start using progesterone for luteal support in FET cycle (day 15), the day of embryo transfer, 6 and 12 weeks of pregnancy. Method of measurement: Blood serum level.;Progesterone. Timepoint: start using progesterone for luteal support in FET cycle (day 15), the day of embryo transfer, 6 and 12 weeks of pregnancy. Method of measurement: Blood serum level.
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