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Clinical Trials/NCT07352189
NCT07352189
Completed
Not Applicable

Comparison of the Efficacy of Ultrasound-Guided and Laparoscopy-Guided Transversus Abdominis Plane(TAP) Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Upper Abdominal Surgery

Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital0 sites60 target enrollmentStarted: January 11, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Enrollment
60

Overview

Brief Summary

This prospective, randomized, double-blind study aimed to compare the effects of ultrasound-guided versus laparoscopy-guided transversus abdominis plane(TAP) block on postoperative analgesia in patients undergoing laparoscopic upper abdominal surgery under general anesthesia. Postoperative pain scores, analgesic consumption and recovery parameters were evaluated during the first 24 hours after surgery.

Detailed Description

Patients aged 18-70 years with ASA physical status I-III who were scheduled for laparoscopic upper abdominal surgery under general anesthesia were included in the study. After induction of anesthesia, patients were randomly assigned to one of two group, bilateral subcostal transversus abdominis plane block was performed under ultrasound-guidance using a local anesthetic mixture before extubation. In the laparoscopy-guided group, bilateral subcostal transversus abdominis plane block was performed under laparoscopic guidance using the same local anesthetic mixture before abdominal closure. Postoperative pain intensity was assessed by using the Numeric Rating Scale (NRS). Total opioid consumption, time to first analgesic requirement, paracetamol consumption, postoperative nausea and vomiting, length of hospital stay, time to ambulation and time to gastrointestinal recovery were recorded during the first 24 hours after surgery. Complications related to the TAP block were also evaluated.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients aged 18-70 yeras
  • ASA physical status I-III
  • Scheduled for laparoscopic upper abdominal surgery
  • Provided written informed consent

Exclusion Criteria

  • Patient refusal
  • Allergy to local anesthetics
  • Coagulopathy
  • Infection at the injection site
  • Severe systemic disease
  • ASA physical status IV-V

Investigators

Sponsor
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Sponsor Class
Other
Responsible Party
Sponsor

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