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Transdermal Nicotine in Female Patients at High Risk for Post Operative Nausea and/or Vomiting (PONV)

Postoperative Nausea and Vomiting Clinical Trial

Official title:
Transdermal Nicotine in Female Patients at High Risk for PONV

Clinical Trial Summary

The purpose of this study is to see if the nicotine patch reduces post operative nausea and/or vomiting (PONV) among non-smoking patients who are at high risk of PONV.

Clinical Trial Description

There are certain known risk factors for post-operative nausea and/or vomiting: the use of opioids during surgery, female gender, laparoscopic surgery, gynecologic surgery, strabismus repair, the use of a general anesthetic, obesity, and non-smoker. Patients with four or more of these risk factors have an 80% occurrence rate of post-operative nausea and/or vomiting and are classified as "high risk". It has been shown that those who use tobacco have about a 50% reduction in post-operative nausea and/or vomiting. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00775749
Study type Interventional
Source Ochsner Health System
Contact
Status Withdrawn
Phase N/A
Start date April 2009
Completion date April 2012
View Details
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