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Clinical Trials/NCT04197206
NCT04197206
Completed
N/A

Evaluation of Ultrasound Guided Costotransverse Block in Breast Canser Surgery Patients

Cigli Regional Training Hospital1 site in 1 country70 target enrollmentJanuary 6, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Cigli Regional Training Hospital
Enrollment
70
Locations
1
Primary Endpoint
24 hours morphine consumption
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Costotransverse block is a novel regional anesthesia technique described a few months ago. It's use for breast surgery has been reported by only one case report in the literature. As the investigators have considered that Costotransverse block can be efficacious for providing postoperative analgesia in the breast surgeries, the investigators have implemented the application of this blockade into practice at the clinic. The main purpose of this study is to evaluate the analgesic effect of ultrasound-guided unilateral costotransverse block in breast cancer surgery.

Registry
clinicaltrials.gov
Start Date
January 6, 2020
End Date
April 29, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Cigli Regional Training Hospital
Responsible Party
Principal Investigator
Principal Investigator

Hakan Aygün

Principal Investigator,

Cigli Regional Training Hospital

Eligibility Criteria

Inclusion Criteria

  • patients undergoing breast canser surgery under general anesthesia ASA I-II

Exclusion Criteria

  • patients undergoing breast surgery under paravertebral block and others morbidly obesity ASA III - IV infection of the skin at the site of needle puncture area patients with known allergies to any of the study drugs coagulopathy recent use of analgesic/steroid drugs

Outcomes

Primary Outcomes

24 hours morphine consumption

Time Frame: 24 hours

morphine consumptions for both group will be recorded

Secondary Outcomes

  • Numeric rating scale for postoperative pain intensity(24 hours)

Study Sites (1)

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