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
| Type | Name | Description |
|---|---|---|
| DRUG | Tapentadol | 75 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. |
| OTHER | Placebo | Placebo 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.