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Clinical Trial Summary

The purpose of this study is to test whether transdermal nicotine reduces pain among women with chronic pelvic pain.


Clinical Trial Description

Potential subjects are female non-smokers presenting to their physicians for treatment of chronic pelvic pain. When consented, the subjects fill out a questionnaire on demographic information and pain experience. The trial is conducted at home over three days. Each subject uses three different levels of nicotine (0mg, 5mg, and 10mg) administered in a random order; the study is double-blinded and patients act as their own controls. Subjects apply the placebo or nicotine patches in the morning and remove them in the evening when they fill out a pain diary for the day. During the study, patients will continue their typical course of pain medication and report pain medication use in the pain diary. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00440505
Study type Interventional
Source Columbia University
Contact
Status Completed
Phase Phase 4
Start date February 2004
Completion date June 2008

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