Ultrasound-Guided Costoclavicular Block in Patients With a BMI > 30

Surgery Clinical Trial

Official title:

Ultrasound-Guided Costoclavicular Block in Patients With a BMI > 30

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03314948
• Other study ID #: 17-006489
• Status: Terminated
• Start date: October 16, 2017
• Est. completion date: September 15, 2019

Study information

• Verified date: January 2022
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The Researchers are trying to determine if Costoclavicular brachial plexus block (CCBPB) can be successfully performed in patients with a body mass index greater than thirty.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: September 15, 2019
• Est. primary completion date: September 15, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

18 to 80 years old, with American Society of Anesthesiologists physical status I to IV, undergoing elective hand or forearm surgery under a BPB will be enrolled for this study.

Exclusion Criteria:

Patient's refusal, American Society of Anesthesiologist physical status greater than IV, pregnancy, neuromuscular disease, prior surgery on the intraclavicular fossa, nerve injury or neurological disorders, bleeding tendency or evidence of coagulopathy, history of allergy to local anesthetic drugs, skin infection at the site of needle insertion, or contraindication to regional anesthesia.

Related Conditions & MeSH terms

• Surgery

Locations

Country	Name	City	State
United States	Mayo Clinic Florida	Jacksonville	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Success rate of costoclavicular brachial plexus block	Determine the success rate of the block in patients with body mass index greater than 30. Assess the effectiveness of the block by performing required assessments	Within 45 minutes of completion of block placement
Secondary	Identification of costoclavicular space	Describe how the costoclavicular space and its contents are easily identifiable in patients with a body mass index greater than 30. Identify the costoclavicular space by using ultrasound	during placement of the block

External Links

•   Mayo Clinic Clinical Trials