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NCT04332497

Clavipectoral Fascia Plane Block Versus Interscalen Brachial Plexus Block for Clavicle Surgery

Withdrawn NA Last updated 27 April 2022
What this trial tests

NA trial testing "Ibuprofen", "Dorifen®"; "Fentanyl", "Talinat®", ''Patient Controlled Analgesia Device'' in Clavicle Fracture. Withdrawn.

Timeline
10 April 2020
Primary endpoint
20 December 2021
30 December 2021

Quick facts

Lead sponsorMedipol University
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Start date10 April 2020
Primary completion20 December 2021
Estimated completion30 December 2021
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Medipol University

Who can join

Adults 18 to 65, any sex, with Clavicle Fracture or Clavicle Injury. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 compare the efficacy of the US-guided CPB and ISCB for postoperative analgesia management after clavicle surgery. The primary aim is to compare perioperative and postoperative opioid consumption and the secondary aim is to evaluate postoperative pain scores (VAS), adverse effects related with opioids (allergic reaction, nausea, vomiting).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Clavicle Fracture

Currently open trials in the same condition.

Other Medipol University trials

Trials by the same sponsor.

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Data sources for this page

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