Actively Recruiting
Motor Sparing Supraclavicular Block
Led by Cairo University · Updated on 2024-05-16
44
Participants Needed
1
Research Sites
31 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to compare MS-SCBPB and SCBPB in the duration of postoperative analgesia, time to first analgesic request (VAS ≥40 mm), pain scores, motor power, and side effects.
CONDITIONS
Official Title
Motor Sparing Supraclavicular Block
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for upper limb surgeries under supraclavicular brachial plexus block
- American Society of Anesthesiologists (ASA) status I and III
- Between 18 and 60 years of age
You will not qualify if you...
- Bleeding disorders with INR greater than 1.5 and/or platelets less than 100,000/mm3
- Infection at the injection site
- Allergy to local anesthetics
- Severe cardiopulmonary disease (ASA IV or higher)
- Diabetic or other neuropathies
- Motor disorders
- Patients receiving opioids for chronic analgesic therapy
- Inability to understand or use the visual analogue scale (VAS) for pain
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cairo university Hospitals. kasralainy
Cairo, Governorate, Egypt, 002
Actively Recruiting
Research Team
N
Nagy malak, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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