Clinical Trials Directory

Trials / Completed

CompletedNCT01062087

Pain Perception After Tubal Ligation

Retrospective Investigation of Postoperative Pain Perception After Laparoscopic Tubal Sterilization

Status
Completed
Phase
Study type
Observational
Enrollment
62 (actual)
Sponsor
Oklahoma State University Center for Health Sciences · Academic / Other
Sex
Female
Age
21 Years – 52 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGBupivacaine, LidocaineInjection at surgical port site of 0.25% Bupivicaine, 2.5 mg/mL NaCl solution and/or application of Lidocaine HCl jelly 2% aqueous, up to 5 mL

Timeline

Start date
2010-01-01
Primary completion
2010-05-01
Completion
2010-12-01
First posted
2010-02-04
Last updated
2012-05-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01062087. Inclusion in this directory is not an endorsement.