A pilot study to assess the feasibility of a RCT to compare the effectiveness of two different progesterone only pills (POP) on reducing pelvic pai

Not Applicable

Completed

• Conditions: rological and Genital Diseases: Pelvic pain; Urological and Genital Diseases; Pelvic pain

• Registration Number: ISRCTN42638345
• Lead Sponsor: Department of Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-09-30
• Last Update Posted: 17 October 2016

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 25

Inclusion Criteria

1. Females over 18 years of age who require a method of contraception
2. Willing to follow protocol
3. Able to give written consent

Exclusion Criteria

Not provided at time of registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified