Effect of tailored versus standard use of the combined oral contraceptive on continuation rates at one year

Completed

• Conditions: nintended pregnancy and abortion; Pregnancy and Childbirth; Unintended pregnancy

• Registration Number: ISRCTN73812769
• Lead Sponsor: Camden Primary Care Trust (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2008-07-31
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 600

Inclusion Criteria

1. Females greater than or equal to 18 and less than or equal to 45 years of age
2. Requesting combined oral contraceptive (COC) as future or ongoing contraceptive method and for this to be an appropriate choice
3. Willing to be randomised to one of the two groups
4. Willing to follow protocol for 12 months
5. Able to give written consent
6. Access to the internet, has an email address and mobile phone
7. Willing to complete an online diary regularly, i.e. weekly, for up to 12 months after starting the allocated regimen

Exclusion Criteria

Any recognised contraindications to COC (UK Medical Eligibility Criteria [UKMEC] points 3 and 4, 2007).

Study & Design

• Study Type: Interventional
• Study Design: Not specified