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Clinical Trials/NCT04634721
NCT04634721
Completed
Not Applicable

Transversus Abdominis Plan Block Applied in Laparoscopic Cholecystectomies Effective By Which Method: Ultrasound or Laparoscopic?

Ankara City Hospital Bilkent1 site in 1 country60 target enrollmentNovember 1, 2020

Overview

Phase
Not Applicable
Intervention
bupivacaine
Conditions
Bupivacaine
Sponsor
Ankara City Hospital Bilkent
Enrollment
60
Locations
1
Primary Endpoint
Mean postoperative static and dynamic numeric rating scale (NRS) at 24 hours
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Abdominal wall blocks are frequently used as part of multimodal analgesia for pain control after abdominal surgery. There are studies using the Transversus Abdominis Plane Block for postoperative pain control in laparoscopic cholecystectomies.

In this study, the investigators aimed to compare the advantages of these two methods by applying the Transversus Abdominis Plan Block for postoperative pain control after laparoscopic cholecystectomy with the help of postoperative USG and laparoscopy during surgery.In this study, the investigators aimed to compare the advantages of these two methods by applying the Transversus Abdominis Plan Block for postoperative pain control after laparoscopic cholecystectomy with the help of postoperative USG and LAPAROSCOPY during surgery.

Detailed Description

A total of 60 patients aged 18-65, ASA 1-2-3, who will undergo elective laparoscopic cholecystectomy in our hospital, will be included in the study. Patients will be randomly divided into 3 groups with ultrasound (USG) guided (GROUP 1: USG) , Laparoscopic application (GROUP 2: LAP) and GROUP 3 :No-TAP blok Each group consists of 20 evil people. Written consent will be obtained by explaining the procedure to be performed before the operation to the patients. The Transversus Abdominis Plan Block will be applied to the patients by a blind anesthesiologist according to their group. The block to be made by the anesthesiologist who will apply the block procedure will be given in a closed envelope.

Registry
clinicaltrials.gov
Start Date
November 1, 2020
End Date
January 15, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mehmet sahap

Principal Investigator

Ankara City Hospital Bilkent

Eligibility Criteria

Inclusion Criteria

  • ASA I,II,III
  • Patients 18-65
  • laparoscopic cholecystectomy

Exclusion Criteria

  • ASA III higher
  • history of pain relief medication dependence
  • history of substance abuse
  • end stage chronic kidney disease
  • advanced liver disease
  • history of chronic pain -history of taking opioids or neuropathic agents regularly prior to surgery-
  • BMI of 50 or over
  • skin infections at the site of TAP block injection or port sites.

Arms & Interventions

Laparoscopic TAP block

Laparoscopic assisted TAP block will be done by surgeon intra-operatively

Intervention: bupivacaine

Ultrasaund TAP block

injecting bupivacaine in transversus abdominis plane to block the somatic nerves

Intervention: bupivacaine

Outcomes

Primary Outcomes

Mean postoperative static and dynamic numeric rating scale (NRS) at 24 hours

Time Frame: 24 hours

o compare the mean NRS at 0hr, 1hr, 2 hrs. 6 hrs. 12 hrs. and 24hrs. post-operatively between three groups Numeric rating scale for pain,(0=no pain, 1-3= mild pain, 4-6 moderate pain, 7-10 severe pain.)

Secondary Outcomes

  • Post operative nausea or vomiting(24 hours)

Study Sites (1)

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