Status:
UNKNOWN
Total Intravenous Anesthesia With Propofol vs. General Anesthesia in Outpatient Shoulder Arthroscopic Surgeries
Lead Sponsor:
Carilion Clinic
Conditions:
Rotator Cuff Tears
Rotator Cuff Injuries
Eligibility:
All Genders
18-75 years
Phase:
PHASE4
Brief Summary
This study is comparing total intravenous anesthesia with propofol with a regional nerve block against general anesthesia with a regional nerve block on the primary endpoint of time to meet discharge ...
Detailed Description
The primary objective of this study is to determine if using Total Intravenous Anesthesia with Propofol (TIVA-P sedation) with a regional nerve block will decrease the time to meet discharge criteria....
Eligibility Criteria
Inclusion
- 18-75 years of age
- Candidate for a shoulder arthroscopic procedure in the beach chair position
Exclusion
- American Society of Anesthesiologists (ASA) level 4 or above
- History of brachial plexus injury
- Chronic Obstructive Pulmonary Disorder
- Unstable Asthma
- BMI greater than 40
- Allergy to local anesthesic (bupivacaine)
- Contralateral phrenic nerve impairment
- History of Difficult Airway
- Poorly Controlled Gastroesophageal Reflux Disease
- Known Aspiration Risk
- Surgery not performed at the Roanoke Ambulatory Surgical Center
- Pregnant patients or patients who have a positive pre-operative human chorionic gonadotropin (beta-HCG) pregnancy test
- Coagulopathies
- Allergy to propofol
- Patient request for specific anesthesia method
Key Trial Info
Start Date :
February 2 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2023
Estimated Enrollment :
192 Patients enrolled
Trial Details
Trial ID
NCT04793022
Start Date
February 2 2021
End Date
August 1 2023
Last Update
February 8 2023
Active Locations (1)
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1
Carilion Clinic Institute of Orthopedics and Neurosurgery
Roanoke, Virginia, United States, 240176