Analgesia for Clavicular Fracture and Surgery

Completed

• Conditions: Clavicular Fractures
• Interventions: Procedure: Interscalene-Cervical Plexus Block; Procedure: Supraclavicular-Cervical Plexus Block

• Registration Number: NCT03933228
• Lead Sponsor: Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Brief Summary

Compared efficacy of ultrasound-guided combined interscalene-cervical plexus versus combined supraclavicular-cervical plexus block for surgical anesthesia in clavicular fractures.

Detailed Description

The primary objective of this study was to compare the effectiveness of ultrasound-guided combined interscalene-cervical plexus versus combined supraclavicular-cervical plexus block for surgical anesthesia in clavicular fractures.The hypothesis of this study was that the supraclavicular-cervical plexus block could provide better anesthesia with less anesthesia related complications.

Study Timeline

• Study First Submitted: 2019-04-28
• Study First Submitted QC: 2019-04-28
• Study Start: 2019-05-01
• Study First Posted: 2019-05-01
• Primary Completion: 2021-12-01
• Study Completion: 2022-03-01
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-08
• Last Update Posted: 2024-04-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

• Surgery of the clavicular fractures under combined cervical plexus plus brachial plexus block
• Urgent or planned surgery

Exclusion Criteria

• Refused to sign informed consent
• Pregnant women
• Allergic to the local anesthetic

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Interscalene-Cervical Plexus Block	Interscalene-Cervical Plexus Block	Ultrasound-Guided Combined Interscalene-Cervical Plexus Block
Supraclavicular-Cervical Plexus Block	Supraclavicular-Cervical Plexus Block	Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Primary Outcome Measures

Name	Time	Method
Block success rate	At time 15 minutes after the block	Sensory blockade was assessed using the pinprick test at the surgery site

Secondary Outcome Measures

Name	Time	Method
Acute complications	At the end of surgery immediately	Number of participants with phrenic nerve palsy

Trial Locations

Locations (1)

Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine; 🇨🇳 Cangzhou, Hebei, China