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OpenTrials
Completed

NCT Number: NCT06269562

SPSIPB and CPB on Clavicle Surgeries

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).

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Serratus posterior superior intercostal plane block and clavipectoral plane block

Procedure

The analgesic effectiveness achieved by the concurrent application of these two techniques was investigated.

Primary outcomes

  1. Numerical Rating Scale

    Time frame: 24 hours after the procedure

    0=no pain , 10= the worst pain

Secondary outcomes

  1. tramadol consumption

    Time frame: 24 hours after the procedure

    total tramadol consumption of patients

Sponsors and collaborators

Lead sponsor

Cumhuriyet University

Other

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Feb 21, 2024
Registry last updated
Feb 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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