MedPath

progestrone effect on pregnancy

Not Applicable
Conditions
Other complications associated with artificial fertilization.
Noninflammatory disorders of female genital tract
Registration Number
IRCT2015010220408N2
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
148
Inclusion Criteria

Inclusion criteria; Women younger than 35 years old with unexplained infertility; Proper ovulation; 2 open tubal; Not having severe or moderate problem of man and without a history of previous abdominal surgery. Exclusion criteria; Advanced endometriosis; Dense pelvic adhesion; Genital TB; Patients who did not reffer for following up.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical pregnancy rate. Timepoint: two weeks after start of intervention. Method of measurement: Transvaginal ultrasonography and pregnancy test.
Secondary Outcome Measures
NameTimeMethod
Miscariage rate. Timepoint: Until 24 weeks after start of intervention. Method of measurement: History, Physical exam, Ultrasonography.;Patients acceptance. Timepoint: Untill 12 weeks. Method of measurement: Questionare.;Progestrone serum level. Timepoint: one week after start of intervention. Method of measurement: measure of blood progestrone.
© Copyright 2025. All Rights Reserved by MedPath