Status:
WITHDRAWN
Effectiveness of Ultrasound (US) Guided Supraclavicular Block
Lead Sponsor:
Baylor College of Medicine
Conditions:
Analgesia
Pain
Eligibility:
All Genders
18-64 years
Phase:
NA
Brief Summary
This research study is being done in order to find out if there is any difference in the effectiveness of ultrasound guided supraclavicular brachial plexus nerve block that can be achieved with 3 diff...
Eligibility Criteria
Inclusion
- Patients between the ages of 18-64,
- Patients who are ASA I-III, presenting for distal upper extremity surgery. Surgeries to be considered are ORIF of distal upper extremity fractures such as ORIF radius, ORIF ulna, ORIF of any bones in the wrist or hand, and distal upper extremity surgery involving bones or tendons for which postoperative pain is to be expected. No emergency surgeries will be considered.
Exclusion
- Emergency surgery,
- Patient or surgeon refusal
- Patients for which peripheral nerve block or study medications are contraindicated,
- Patients on chronic analgesic therapy at home,
- History of nerve injury, neuropathy, or known neurologic injury or illness, or inability to properly describe postoperative pain to investigators (language barrier, psychiatric disorder, dementia).
Key Trial Info
Start Date :
May 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00923494
Start Date
May 1 2009
End Date
December 1 2010
Last Update
January 20 2017
Active Locations (1)
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1
Ben Taub General Hospital
Houston, Texas, United States, 77030