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Clinical Trials/NCT03741452
NCT03741452
Completed
N/A

Evaluation of Ultrasound-guided Transversalis Fascia Plane Block for Postoperative Analgesia in Cesarean Section: A Prospective, Randomized, Controlled Clinical Trial

Maltepe University1 site in 1 country70 target enrollmentNovember 26, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Maltepe University
Enrollment
70
Locations
1
Primary Endpoint
24 hours tramadol consumption
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Transversalis fascia plane block is a regional anesthesia technique described ten years ago. Its use for many indications has been identified by case reports in the literature. As the investigators have considered that transversalis fascia plane block could be efficacious for providing postoperative analgesia in the cesarean section, 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 bilateral transversalis fascia plane block in cesarean section.

Registry
clinicaltrials.gov
Start Date
November 26, 2018
End Date
February 22, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Asst. Prof. Serkan Tulgar, M.D.

assoc professor in anesthesiology and reanimation

Maltepe University

Eligibility Criteria

Inclusion Criteria

  • patients undergoing cesarean section under general anesthesia ASA I-II

Exclusion Criteria

  • patients undergoing cesarean section under neuraxial anesthesia 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 drugs

Outcomes

Primary Outcomes

24 hours tramadol consumption

Time Frame: 24 hour

tramadol consumptions for both group will be recorded

Secondary Outcomes

  • Numeric rating scale for postoperative pain intensity(24 hours)
  • Postoperative nausea and vomiting(24 hours)

Study Sites (1)

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