The Effect of Dexamethasone Adjuvant to Varying Doses of Bupivacaine on Motor and Sensory Blockade in Infraclavicular Brachial Plexus Blockade

Not Applicable

Active, not recruiting

• Conditions: Infraclavicular Brachial Plexus Block; Dexamethasone Administration; Bupivacaine

• Registration Number: NCT06769581
• Lead Sponsor: Gaziosmanpasa Research and Education Hospital

Brief Summary

This single-center, prospective, randomized, double-blinded controlled trial investigates the effects of adding 4 mg dexamethasone to different concentrations of bupivacaine on motor and sensory block duration in infraclavicular brachial plexus block. A total of 120 ASA I-II patients aged 18-65 undergoing elective surgeries of the hand, wrist, forearm, or elbow will be randomly assigned to one of four groups:

Group 1: 25 mL of 0.5% bupivacaine. Group 2: 25 mL of 0.5% bupivacaine with 4 mg dexamethasone. Group 3: 25 mL of 0.375% bupivacaine with 4 mg dexamethasone. Group 4: 25 mL of 0.25% bupivacaine with 4 mg dexamethasone. The infraclavicular block will be performed using a lateral sagittal approach under ultrasound and nerve stimulator guidance. Primary outcomes include the duration of motor and sensory block, assessed with a motor block scale and pin-prick sensory test. Secondary outcomes include block onset times, postoperative pain scores (Visual Analog Scale), total analgesic consumption within 48 hours, time to first postoperative analgesic, and rates of rescue block or conversion to general anesthesia.

This study aims to evaluate whether combining dexamethasone with lower concentrations of bupivacaine can maintain block efficacy while reducing local anesthetic dosage, potentially improving the safety and effectiveness of peripheral nerve block protocols.

Detailed Description

This study investigates whether adding dexamethasone, a commonly used steroid, to different strengths of bupivacaine (a local anesthetic) can improve the effectiveness and duration of nerve blocks used for upper limb surgeries. The nerve block in this study is an infraclavicular brachial plexus block, which numbs the arm and hand by targeting specific nerves near the shoulder. This type of anesthesia is often preferred for surgeries of the hand, wrist, forearm, or elbow because it reduces pain and the need for general anesthesia.

What Is Being Studied? The research focuses on four groups of patients receiving different mixtures of bupivacaine, with or without dexamethasone. Each patient will receive the same volume of anesthetic solution (25 mL) through a standardized procedure performed under ultrasound and nerve stimulator guidance.

* Group 1: 0.5% bupivacaine only.

* Group 2: 0.5% bupivacaine with 4 mg dexamethasone.

* Group 3: 0.375% bupivacaine with 4 mg dexamethasone.

* Group 4: 0.25% bupivacaine with 4 mg dexamethasone. Why Is This Important? Local anesthetics like bupivacaine can effectively block pain, but using higher concentrations may carry risks, such as muscle weakness or local anesthetic toxicity. Combining dexamethasone with lower concentrations of bupivacaine might extend the block's duration and effectiveness, potentially reducing the total amount of anesthetic needed. This could improve patient safety and recovery while maintaining excellent pain control.

How Will It Be Done? The study involves 120 adult patients aged 18-65, all undergoing elective upper limb surgeries. Participants will be randomly assigned to one of the four groups, and both the patients and the doctors evaluating their progress will not know which group they are in.

Before surgery, each patient will receive the nerve block. The anesthetic solution will be injected near the shoulder, targeting specific nerves with the help of ultrasound and a nerve stimulator. Researchers will measure:

* How quickly the block starts working (block onset time).

* How long the block lasts (motor and sensory block duration).

* The level of pain experienced after surgery, using a pain scale.

* The total amount of pain medication needed within the first 48 hours. What Happens After Surgery? Patients will be closely monitored for pain and block effectiveness. If a patient experiences significant pain during surgery due to an incomplete block, additional anesthetic may be given to the specific nerve, or general anesthesia may be initiated if necessary. Postoperatively, pain relief will be managed with standard medications, and the timing and total dosage will be recorded.

Study Goals:

The primary goal is to determine whether dexamethasone can enhance the duration and effectiveness of the block across different bupivacaine strengths. Secondary goals include understanding how dexamethasone affects block onset time, postoperative pain, and the need for additional pain medications.

Broader Implications:

The findings could help refine anesthesia techniques, making nerve blocks safer and more effective. If lower concentrations of bupivacaine combined with dexamethasone provide similar or better results than higher concentrations alone, this could reduce the risks associated with local anesthetics and improve patient recovery experiences.

This research has the potential to guide future anesthesia practices, benefiting both patients and clinicians by optimizing drug combinations for nerve blocks.

Study Timeline

• Study Start: 2024-01-02
• Primary Completion: 2024-08-01
• Status Verified: 2025-01
• Study First Submitted: 2025-01-06
• Study First Submitted QC: 2025-01-06
• Last Update Submitted: 2025-01-06
• Study First Posted: 2025-01-10
• Last Update Posted: 2025-01-10
• Study Completion: 2025-02-01

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

• Patients aged 18-65 years with ASA I-II who will undergo surgery on the hand, wrist, forearm, or elbow.

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Exclusion Criteria

• Patient refusal to undergo the procedure
• ASA III or higher status
• Diagnosis of diabetes mellitus
• Pregnancy
• History of multiple trauma
• Patients with communication difficulties during or after the procedure
• Sensory impairment at the site of regional anesthesia application
• Presence of a neuromuscular disease
• Open wound or infection at the site of block application
• Coagulopathy that contraindicates the block
• History of allergy to the drugs to be used

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Duration of motor and sensory block	48 hours	The primary outcome of this study is to examine the effects of different concentrations of bupivacaine combined with dexamethasone, in the same volume, on the duration of motor block and sensory block during infraclavicular brachial plexus block.

Secondary Outcome Measures

Name	Time	Method
Block Onset Time	30 minutes	The secondary outcome of this study is the onset time of infraclavicular brachial plexus block.
Postoperative pain levels	48 hours	Evaluating the postoperative pain levels in patients. Pain levels will be assessed using the Visual Analog Scale (VAS).
Total analgesic requirements	48 hours	Evaluating the total analgesic requirements during the first 48 hours postoperatively.
Block Failure	30 minutes	Comparing the rates of rescue blocks and the incidence of conversion to general anesthesia following the administration of infraclavicular brachial plexus block.

Trial Locations

Locations (1)

Gaziosmanpasa Training and Research Hospital; 🇹🇷 Istanbul, Turkey