Clinical Trials Directory

Trials / Completed

CompletedNCT07320781

Role of Preoperative Tapentadol in Reduction of Perioperative Analgesic Requirement After Breast Conservative Surgery in Cancer Patients.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Shaukat Khanum Memorial Cancer Hospital & Research Centre · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study evaluated the preemptive analgesic efficacy of Tapentadol in reducing peri operative analgesic requirements among patients undergoing breast cancer surgery.

Detailed description

A double blinded prospective RCT was conducted with 70 patients undergoing breast cancer surgery with 35 patients being studied with Administrated drug \& other 35 as placebo. Intraoperative \& postoperative morphine consumption was calculated and documented.

Conditions

Interventions

TypeNameDescription
DRUGTapentadol75 mg oral tapentadol given 1 hour before surgery in control group and placebo tablet was given in Group B. Intraoperative and post operative morphine consumption and pain scores at 1,2,3,4 hours were calculated.
OTHERPlaceboPlacebo tablet was given in group B.

Timeline

Start date
2024-11-15
Primary completion
2025-09-30
Completion
2025-10-10
First posted
2026-01-06
Last updated
2026-01-08

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT07320781. Inclusion in this directory is not an endorsement.

Role of Preoperative Tapentadol in Reduction of Perioperative Analgesic Requirement After Breast Conservative Surgery in (NCT07320781) · Clinical Trials Directory