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Due to lack of resources and changes in current practice, the study was terminated
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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.
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| Measure | Description | Time Frame |
|---|---|---|
| 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 |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
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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.
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All patients undergoing an elective hand or forearm surgery
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| Name | Affiliation | Role |
|---|---|---|
| Christopher Robards, MD | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic Florida | Jacksonville | Florida | 32224 | United States |
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| Label | URL |
|---|---|
| Mayo Clinic Clinical Trials | View source |
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