Randomised controlled trial of condoms plus additional lubricatio

Completed

• Conditions: Contraception; Pregnancy and Childbirth; Preventing condom failure

• Registration Number: ISRCTN59655786
• Lead Sponsor: HS R&D Regional Programme Register - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-01-23
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 290

Inclusion Criteria

Couples over the age of 18 years and intend to use condoms regularly and who do not use additional lubricant with them.

Exclusion Criteria

1. Subjects who are not willing to be randomised or to use additional lubricant with their condoms
2. Subjects unlikely to allow follow-up or co-operate with outcome data collection
3. Subjects without a regular partner
4. Couples with a known sensitivity to spermicides or latex
5. Couples who are not intending to use condoms at least predominantly for vaginal intercourse

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Condom failure

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration