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Effects of clomiphene and tamoxifen on pregnancy rate in infertile wome

Phase 2
Conditions
Ovarian dysfunction, unspecified.
Ovarian dysfunction, unspecified
Registration Number
IRCT201206131306N3
Lead Sponsor
Vice chancellor for research-Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
144
Inclusion Criteria

Inclusion criterion: infertile women with ovulation disorders without other cause of infertility. Exclusion criteria: abnormal semen analysis and HSG or laparoscopy; age over 40; myoma; hyperprolactinema; FSH over12; hypothyroidism; hyperthyroidism; previous history of induction of ovulation; renal & liver disease and contraindication of clomiphen citrate and tamoxifen.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pregnancy rate. Timepoint: End of menstural cycle. Method of measurement: Serum BhCG.
Secondary Outcome Measures
NameTimeMethod
Abortion rate. Timepoint: End of menstrual cycle. Method of measurement: The incidence of menstrual bleeding and new.;Multigestation rate. Timepoint: End of menstrual cycle. Method of measurement: Sonography.;Ovarian hyperstimulation syndrome. Timepoint: End of menstrual cycle. Method of measurement: Clinical and ultrasound.;Side effects such as headaches, dizziness, blurred vision, nausea and vomiting. Timepoint: During the treatment cycle. Method of measurement: Ask the patient.
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