Nicotine Administration and Post-operative Opioid Use With Bariatric Surgery

Completed · Phase 4

Conditions studied: Pain, Postoperative

In brief

This prospective, randomized, double-blind study will enroll nonsmoking female subjects undergoing laparoscopic bariatric surgery under general anesthesia. The hypothesis of this study is that female nonsmokers who receive nicotine via nasal spray immediately before waking up from anesthesia will need less pain medications 24 hours after the surgery compared to the subjects who receive placebo spray.

Key facts

Study ID
NCT01194089
Run by
Toby Weingarten
People needed
95
Starts
2010-08-01
Expected to finish
2014-04-01
Last updated by the study team
2015-07-09

Who can join

Age: 18 and older, up to 60. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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