Clinical Trials Directory

Trials / Terminated

TerminatedNCT03796403

Bupivacaine Plus Diclofenac Versus Bupivacaine Alone for Postoperative Pain Relief in Gynecologic Cancer Patients

Comparison of Bupivacaine Peritoneal Infiltration and Intramuscular Diclofenac Versus Bupivacaine Peritoneal Infiltration Alone for Postoperative Pain Relief in Gynecologic Cancer Patients Undergoing Open Surgery

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Department of Medical Services Ministry of Public Health of Thailand · Other Government
Sex
Female
Age
21 Years – 70 Years
Healthy volunteers
Not accepted

Summary

compare the postoperative pain between Bupivacaine peritoneal Infiltration plus immediately postoperative intramuscular Diclofenac and Bupivacaine peritoneal infiltration alone by using visual analogue score (VAS).

Detailed description

The primary objective is to compare the postoperative pain between Bupivacaine peritoneal Infiltration plus immediately postoperative intramuscular Diclofenac and Bupivacaine peritoneal infiltration alone by using visual analogue score (VAS). The secondary objective is to evaluate the time to first dose and the total amount of morphine requirement after the operation in both groups.

Conditions

Interventions

TypeNameDescription
OTHERDiclofenacTwenty mL of bupivacaine was infiltrated into surgical-site peritoneum , divided in 10 sites before closure, and diclofenac 75 mg (3 mL) was intramuscularly injected immediately after complete the procedure and the operative field was covered with sterile adhesive wound dressing.

Timeline

Start date
2019-02-15
Primary completion
2019-09-30
Completion
2019-12-30
First posted
2019-01-08
Last updated
2020-10-23

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT03796403. Inclusion in this directory is not an endorsement.