The effect of dydrogesterone and vaginal progestrein in support of artificial reproduction techniques

Not Applicable

• Conditions: In vitro fertilization.; Complications of attempted introduction of fertilized ovum following in vitro fertilization; N98.2

• Registration Number: IRCT20170205032406N2
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 210

Inclusion Criteria

20-40 years old
Body Mass Index 18-30 kg/m2
Endometrium Thickness 7-14 mm

Exclusion Criteria

Abnormal prolactin serum level and abnormal thyroid function test
Diminished ovarian reserve ( baseline FSH level >10 IU/mL)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pregnancy. Timepoint: Once a week after embryo transfer into the patient. Method of measurement: The blood hCG test.

Secondary Outcome Measures

Name	Time	Method
Preterm delivery. Timepoint: Every two weeks from the twentieth week of pregnancy. Method of measurement: Patient visit and record uterine contractions.;Amount of live birth. Timepoint: Every two weeks from twenty-eighth week of pregnancy. Method of measurement: Patient visit and record baby's birth.;Abortion. Timepoint: Six weeks after intervention. Method of measurement: Sonography and pregnancy test.