SPSIPB and CPB on Clavicle Surgeries

Not Applicable

Completed

• Conditions: Analgesia; Clavicle Fracture; Postoperative Pain
• Interventions: Procedure: Serratus posterior superior intercostal plane block and clavipectoral plane block

• Registration Number: NCT06269562
• Lead Sponsor: Cumhuriyet University

Brief Summary

Clavicular fractures represent a common occurrence often necessitating effective pain management strategies, particularly following surgical interventions. This study involved a cohort of five patients who underwent clavicular fracture surgery under general anesthesia. A novel analgesic approach combining two distinct nerve block techniques-Serratus Posterior Superior Intercostal Plane Block (SPSIPB) and Clavipectoral Plane Block (CPB)-was employed for postoperative pain control. The procedural methodology encompassed the administration of SPSIPB preceding anesthesia induction, followed by CPB subsequent to induction. SPSIPB targeted specific neural regions responsible for sensory blockade within the innervation of the clavicular skin, whereas CPB focused on the clavipectoral fascia. Standard anesthesia protocols were utilized, and postoperative pain levels were evaluated using Numeric Rating Scores (NRS).

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-20
• Primary Completion: 2023-12-20
• Status Verified: 2024-02
• Study Completion: 2024-02-04
• Study First Submitted: 2024-02-06
• Study First Submitted QC: 2024-02-13
• Last Update Submitted: 2024-02-13
• Study First Posted: 2024-02-21
• Last Update Posted: 2024-02-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

• Five American Society of Anesthesiologists (ASA) Ⅰ-II- III patients scheduled for clavicle surgery will be included in the study

Exclusion Criteria

• patients with bleeding disorders
• patients with signs of infection in the block application area
• patients with unstable haemodynamics
• patients with thyroid cardiovascular, renal, hepatic and neuropsychiatric diseases
• patients with vascular disease,
• patients with respiratory distress
• patients whose consent for the study could not be obtained or who did not accept to participate in the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Block	Serratus posterior superior intercostal plane block and clavipectoral plane block	consists of 5 patients in whom both techniques were applied

Primary Outcome Measures

Name	Time	Method
Numerical Rating Scale	24 hours after the procedure	0=no pain , 10= the worst pain

Secondary Outcome Measures

Name	Time	Method
tramadol consumption	24 hours after the procedure	total tramadol consumption of patients

Trial Locations

Locations (1)

Sivas Cumhuriyet University; 🇹🇷 Sivas, Turkey