Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery
Recruiting
N/AInterventional Study
Pain ManagementAnaesthesia Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
60 (estimated)
Sponsor
Gaziosmanpasa Research and Education Hospital · Government
Who this trial is looking for
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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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* ASA 1-2
* Body Mass Index (BMI) of 18-35 kg/m²
* Age: 18-65 years -Patients undergoing all upper extremity orthopedic surgeries, except shoulder surgeries (distal humerus, elbow, forearm, hand, and wrist), will be included. -
Exclusion Criteria:
* Patient refusal
* Pregnancy…
Inclusion Criteria:
* ASA 1-2
* Body Mass Index (BMI) of 18-35 kg/m²
* Age: 18-65 years -Patients undergoing all upper extremity orthopedic surgeries, except shoulder surgeries (distal humerus, elbow, forearm, hand, and wrist), will be included. -
Exclusion Criteria:
* 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 \>35
* Severe cardiovascular, renal, or hepatic disease
* Infection at the site of the nerve block
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