Actively Recruiting
Impact of Bupivacaine Dilution With Dextrose or Saline on Infraclavicular Block Outcomes
Led by Burçin Alaçam, MD · Updated on 2026-03-11
90
Participants Needed
1
Research Sites
18 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
D5W) has long been used as an intravenous fluid for hydration and energy supplementation and has recently gained increasing clinical interest in perineural injection therapies and ultrasound-guided hydrodissection. D5W has been shown to improve pain and functional outcomes in entrapment neuropathies by mechanically releasing perineural adhesions and potentially modulating neurogenic inflammation. In contrast, 0.9% sodium chloride (normal saline) is routinely used as a dilution medium for local anesthetics in peripheral nerve blocks; however, emerging evidence suggests that alternative diluents such as D5W may influence block onset and efficacy. The infraclavicular block is a commonly used ultrasound-guided technique for brachial plexus anesthesia, providing reliable anesthesia and postoperative analgesia for upper extremity surgery. This study aims to compare the effects of diluting bupivacaine with either D5W or 0.9% NaCl on block success and duration of analgesia in patients undergoing infraclavicular block. Secondary outcomes include block onset characteristics, sensory and motor block profiles, and perioperative analgesic requirements. The findings may help determine whether D5W represents a safe and effective alternative diluent to saline in routine regional anesthesia practice.
CONDITIONS
Official Title
Impact of Bupivacaine Dilution With Dextrose or Saline on Infraclavicular Block Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who agree to participate and provide written informed consent
- Scheduled for elective upper extremity surgery suitable for infraclavicular block anesthesia
- Age between 18 and 65 years
- American Society of Anesthesiologists (ASA) physical status I-III
- Normal neurological exam of the arm planned for the block
You will not qualify if you...
- Patients who do not agree to participate or refuse consent
- History of allergy or hypersensitivity to study medications
- Body mass index of 30 kg/m² or higher
- Body weight less than 40 kg
- Age younger than 18 or older than 65 years
- History of significant cardiac disease such as arrhythmia or conduction disorders
- Blood clotting disorders or platelet count below 100,000/mm³
- Liver failure or major liver dysfunction
- Pregnant women
- Infection at the planned block site
- Neurological deficits in the arm planned for the block
- Uncontrolled diabetes or diabetic neuropathy
- ASA physical status IV
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sakarya University-Anesthesiology and Reanimation Department
Sakarya, Turkey (Türkiye), 54100
Actively Recruiting
Research Team
B
Burçin Alaçam
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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