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Clinical Trials/NCT01062087
NCT01062087
Completed
Not Applicable

Retrospective Investigation of Postoperative Pain Perception After Laparoscopic Tubal Sterilization

Oklahoma State University Center for Health Sciences1 site in 1 country62 target enrollmentJanuary 2010

Overview

Phase
Not Applicable
Intervention
Bupivacaine, Lidocaine
Conditions
Pain
Sponsor
Oklahoma State University Center for Health Sciences
Enrollment
62
Locations
1
Primary Endpoint
Amount of postoperative narcotic required before dismissal from hospital
Status
Completed
Last Updated
14 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
December 2010
Last Updated
14 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Oklahoma State University Center for Health Sciences
Responsible Party
Principal Investigator
Principal Investigator

Sarah McCoy

OB/GYN

Oklahoma State University Center for Health Sciences

Eligibility Criteria

Inclusion Criteria

  • Female, age 21-52,having a laparoscopic tubal ligation by the fallopia ring method at Oklahoma State University Medical Center between January 1, 2005 and December 31, 2009

Exclusion Criteria

  • We will exclude women with the following comorbid conditions, since they may alter the patient's pain level or her perception of pain after the tubal ligation: history of chronic pelvic pain, history of pelvic inflammatory disease, opiate abuse, conversion to open procedure, unsuccessful tubal ligation, laceration of tube, more than one ring placed on single tube, admittance to the hospital, additional procedures performed, endometriosis, allergy to marcaine, lidocaine, or bupivicaine.

Arms & Interventions

Local anesthetic

Women who received local anesthetic during surgery in addition to general anesthesia

Intervention: Bupivacaine, Lidocaine

Outcomes

Primary Outcomes

Amount of postoperative narcotic required before dismissal from hospital

Time Frame: up to 12 hours

Secondary Outcomes

  • The amount of time required for postoperative hospitalization before dismissal(2-12 hours)

Study Sites (1)

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