NCT03259243View on ClinicalTrials.gov

Comparison of Efficacy of Bupivacaine for Relief Postoperative Pain in Women Undergoing Laparoscopic Gynecologic Surgery

PHASE4CompletedINTERVENTIONAL

Enrollment

100

Participants

Timeline

Start Date

April 1, 2017

Primary Completion Date

October 30, 2017

Study Completion Date

January 31, 2018

Conditions

Postoperative Pain Score

Interventions

DRUG

Bupivacaine Hydrochloride

0.5 Bupivacaine hydrochloride were port site infiltration preincision and preclosure injection

Trial Locations (1)

10400

Waetasleem Chema, Bangkok

All Listed Sponsors

lead

Department of Medical Services Ministry of Public Health of Thailand

OTHER_GOV

NCT03259243 - Comparison of Efficacy of Bupivacaine for Relief Postoperative Pain in Women Undergoing Laparoscopic Gynecologic Surgery | Biotech Hunter | Biotech Hunter