Comparison acupuncture with Clomiphene for ovulation induction in polycystic ovary syndrome

Not Applicable

• Conditions: Polycystic Ovary Syndrome.; Polycystic ovarian syndrome; F28.2

• Registration Number: IRCT201512057265N3
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

Patients with infertility and polycystic ovary syndrome

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Ovulation. Timepoint: Every three days since subjects entered the study. Method of measurement: Serial vaginal ultrasonography.