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Clinical Trials/NCT06626191
NCT06626191
Completed
Not Applicable

Comparison of the Postoperative Analgesic Efficacy of Serratus Posterior Superior Intercostal Plane Block and Interscalene Brachial Plexus Block in Shoulder Arthroscopy

Ankara Etlik City Hospital1 site in 1 country90 target enrollmentOctober 8, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Arthroscopy
Sponsor
Ankara Etlik City Hospital
Enrollment
90
Locations
1
Primary Endpoint
Pain Scores
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

Shoulder arthroscopy is one of the common surgical procedures performed today. After shoulder surgery, providing adequate analgesia is necessary for both the comfort of the patient and the ability to perform the necessary post-operative rehabilitation exercises early and regularly.

Nerve blocks reduces opioid consumption in the postoperative period by providing better pain control and therefore has advantages such as fewer side effects and less risk of pulmonary and cardiac complications.

In this study; it was aimed to compare the analgesic effectiveness of interscalene brachial plexus block and serratus posterior superior intercostal plane block, with each other and with the control group in the postoperative period in patients who underwent shoulder arthroscopy.

Registry
clinicaltrials.gov
Start Date
October 8, 2024
End Date
January 14, 2026
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ankara Etlik City Hospital
Responsible Party
Principal Investigator
Principal Investigator

Atakan Sezgi

Principal İnvestigator

Ankara Etlik City Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients aged 18-80 years
  • American Society of Anesthesiologists (ASA) score I-II-III
  • Body Mass Index (BMI) between 18-30 kg/m2

Exclusion Criteria

  • Patients under 18 and over 80 years of age
  • ASA score IV and above
  • Patients with a history of bleeding diathesis
  • BMI below 18 or above 30 kg/m2

Outcomes

Primary Outcomes

Pain Scores

Time Frame: 24 hours after surgery

Pain will be assessed at rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). Pain assessment will be done at 0st, 1st, 2nd,4th, 12th, and 24th hours after surgery.

Secondary Outcomes

  • Intraoperative remifentanil consumption Intraoperative opioid consumption(Intraoperative period)
  • Postoperative Tramadol Consumption(24 hours after surgery)

Study Sites (1)

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