Analgesia for Clavicular Fracture and Surgery

Clavicular Fractures Clinical Trial

Official title:

Ultrasound-Guided Combined Interscalene-Cervical Plexus Versus Combined Supraclavicular-Cervical Plexus Block for Surgical Anesthesia in Clavicular Fractures: A Retrospective Observational Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03933228
• Other study ID #: 2019CZTCWM4
• Status: Completed
• Start date: May 1, 2019
• Est. completion date: March 1, 2022

Study information

• Verified date: April 2024
• Source: Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: March 1, 2022
• Est. primary completion date: December 1, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Clavicular Fractures
• Fractures, Bone

Intervention

Procedure:
• Interscalene-Cervical Plexus Block
Ultrasound-Guided Combined Interscalene-Cervical Plexus Block
• Supraclavicular-Cervical Plexus Block
Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Locations

Country	Name	City	State
China	Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine	Cangzhou	Hebei

Sponsors (1)

Lead Sponsor	Collaborator
Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Block success rate	Sensory blockade was assessed using the pinprick test at the surgery site	At time 15 minutes after the block
Secondary	Acute complications	Number of participants with phrenic nerve palsy	At the end of surgery immediately