Actively Recruiting
Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery
Led by Gaziosmanpasa Research and Education Hospital · Updated on 2025-03-05
60
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
aim of this study is to compare the effect of selective truncal blocks, performed at different doses and volumes, on the onset times of motor and sensory blocks required for anesthesia in patients scheduled for hand, wrist, forearm, and elbow surgeries. Completing the operation under regional anesthesia will be considered a successful block.
CONDITIONS
Official Title
Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- ASA 1-2
- Body Mass Index (BMI) of 18-35 kg/m82
- Age between 18 and 65 years
- Undergoing upper extremity orthopedic surgeries except shoulder surgeries (distal humerus, elbow, forearm, hand, and wrist)
You will not qualify if you...
- Patient refusal
- Pregnancy or breastfeeding
- Severe pulmonary disease
- Contralateral diaphragm paralysis
- Nerve injury secondary to trauma
- Neuromuscular disease
- Peripheral neuropathy
- Bleeding diathesis
- Allergy to local anesthetics and dexamethasone
- Uncontrolled diabetes mellitus
- Morbid obesity with BMI over 35
- Severe cardiovascular, renal, or hepatic disease
- Infection at the site of the nerve block
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Gaziosmanpasa Research and Training Hospital
Istanbul, Turkey (Türkiye), 34255
Actively Recruiting
Research Team
S
serpil Sehirlioglu, MD
CONTACT
D
DONDU GENC MORALAR, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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