Pain Clinical Trial - Pain Perception After Tubal Ligation

Status Completed

Clinical Trial Summary

The purpose of this study is to attempt to determine retrospectively whether there was a statistically significant difference in patient need for postoperative narcotics between two different groups of women who received a laparoscopic tubal ligation. One group received a local anesthetic injection or gel at the surgical sites, in addition to general anesthesia. The other group did not receive any local anesthetic but did receive general anesthesia. The investigators hypothesize that the group that received the local anesthetic injection or gel had lower average postoperative narcotic requirements and shorter postoperative dismissal to home times than the group that did not receive the auxiliary local anesthetic.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Pain

Clinical Trial Details

NCT number	NCT01062087
Study type	Observational
Source	Oklahoma State University Center for Health Sciences
Contact
Status	Completed
Phase	N/A
Start date	January 2010
Completion date	December 2010

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