SPSIPB and CPB on Clavicle Surgeries

Postoperative Pain Clinical Trial

Official title:

Postoperative Analgesic Efficacy of Clavipectoral Plan Block and Serratus Posterior Superior Intercostal Plane Block Combination in Clavicle Surgeries: A Report of Five Cases

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06269562
• Other study ID #: clavicle
• Status: Completed
• Phase: N/A
• Start date: June 20, 2023
• Est. completion date: February 4, 2024

Study information

• Verified date: February 2024
• Source: Cumhuriyet University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: February 4, 2024
• Est. primary completion date: December 20, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Five American Society of Anesthesiologists (ASA) ?-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

Related Conditions & MeSH terms

• Analgesia
• Clavicle Fracture
• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• Serratus posterior superior intercostal plane block and clavipectoral plane block
The analgesic effectiveness achieved by the concurrent application of these two techniques was investigated.

Locations

Country	Name	City	State
Turkey	Sivas Cumhuriyet University	Sivas

Sponsors (1)

Lead Sponsor	Collaborator
Cumhuriyet University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Numerical Rating Scale	0=no pain , 10= the worst pain	24 hours after the procedure
Secondary	tramadol consumption	total tramadol consumption of patients	24 hours after the procedure