SPSIPB and CPB on Clavicle Surgeries

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

5 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-20

Study Completion Date

2024-02-04

Brief Summary

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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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Detailed Description

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Conditions

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Clavicle Fracture Postoperative Pain Analgesia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Block

consists of 5 patients in whom both techniques were applied

Group Type EXPERIMENTAL

Serratus posterior superior intercostal plane block and clavipectoral plane block

Intervention Type PROCEDURE

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

Interventions

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Serratus posterior superior intercostal plane block and clavipectoral plane block

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

Intervention Type PROCEDURE

Eligibility Criteria

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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

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes