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

S

Shaukat Khanum Memorial Cancer Hospital & Research Centre

Status

Completed

Conditions

Breast Cancer

Treatments

Drug: Tapentadol
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT07320781
IRB-23-20

Details and patient eligibility

About

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

Full 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.

Enrollment

70 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18-60 years
  2. ASA 1,2,3
  3. Patients scheduled for breast conservation surgery -

Exclusion criteria

  1. Patient refusal
  2. CKD greater than 3
  3. BMI greater than 35
  4. Known drug allergy -

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups, including a placebo group

Tapentadol
Active Comparator group
Description:
Control drug (Tapentadol )
Treatment:
Drug: Tapentadol
Placebo
Placebo Comparator group
Description:
Placebo sodium bicarbonate/ peppermint oil tablet
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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