WithdrawnNot Applicable

Clavipectoral Fascia Plane Block for Clavicle Surgery

Stopped: no participants

Turkey (Türkiye)0Started 2020-04-22

Plain-language summary

The pain after clavicle fracture surgery may be managed with combined superficial cervical plexus-interscalene block and recently clavipectoral fascia plane block (CPB). CPB was defined by Valdes in 2017 firstly. It may be used for postoperative analgesia after clavicle surgery. CPB may be an alternative to interscalene brachial plexus block. The aim of this study is to evaluate the efficacy of the US-guided CPB for postoperative analgesia management compare to no intervention control group after clavicle surgery. The primary aim is to compare postoperative opioid consumption and the secondary aim is to evaluate postoperative pain scores (VAS), adverse effects related with opioids (allergic reaction, nausea, vomiting).

Who can participate

Age range18 Years – 65 Years

SexALL

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Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I-II * Scheduled for clavicle surgery under general anesthesia Exclusion Criteria: * history of bleeding diathesis, * receiving anticoagulant treatment, * known local anesthetics and opioid allergy, * infection of the skin at the site of the needle puncture, * pregnancy or lactation, * patients who do not accept the procedure

What they're measuring

Opioid consumption

Timeframe: Change from baseline opioid consumption at postoperative 1, 2, 4, 8, 16, 24 and 48 hours

Trial details

NCT IDNCT04328558

SponsorMedipol University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-12-20

View on ClinicalTrials.gov More Clavicle Injury trials