Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID05649644

Sensorimotor Block Dynamics and Hemidiaphragmatic Palsy: A Randomized Superiority Trial Comparing Selective Trunk Block and Supraclavicular Brachial Plexus Block

Led by Chinese University of Hong Kong · Updated on 2025-04-13

50

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are comparing two types of ultrasound-guided nerve blocks used for anesthesia during upper extremity surgeries, which include operations from the shoulder to the hand. The study aims to evaluate whether the Selective Trunk Block (SeTB), which targets the three trunks of the brachial plexus with smaller doses of local anesthetic, provides better anesthesia coverage and fewer complications like hemidiaphragmatic palsy compared to the commonly used supraclavicular brachial plexus block (BPB). This is important because the supraclavicular BPB may not effectively anesthetize all nerve areas and can require larger anesthetic volumes that carry risks for some patients. Participants will be randomly assigned to receive either the SeTB or the supraclavicular BPB. The SeTB involves two skin punctures with three separate injections targeting each trunk of the brachial plexus, using specific mixtures and volumes of local anesthetics. The supraclavicular BPB is performed with a single ultrasound view and injections near the brachial plexus clusters using similar anesthetic mixtures but in different amounts and locations. Both procedures are done with the patient lying on their back with the arm and neck positioned appropriately. Throughout the study, participants will be monitored closely for sensory and motor nerve blockade, the effect on diaphragm function, and any complications during and after the nerve block up to 45 minutes. Researchers will measure readiness for surgery by checking changes in sensation and movement, assess any breathing changes related to nerve involvement, and record secondary outcomes such as block performance time, discomfort, and need for additional pain relief during surgery. The study includes adults aged 18 to 75 undergoing upper arm surgeries and follows a detailed protocol to compare the two anesthesia techniques.

CONDITIONS

Brief Title

Sensorimotor Block Dynamics and Hemidiaphragmatic Palsy: Selective Trunk Block vs Supraclavicular Brachial Plexus Block

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ASA 1-3 patients
  • Undergoing elective or emergency upper extremity surgery involving anywhere from the proximal humerus to distal hand or surgery involving any combination of these regions
  • Age between 18 and 75 years
  • Both males and females
Not Eligible

You will not qualify if you...

  • Patient refusal
  • Pregnancy
  • Skin infection at the site of block placement
  • History of allergy to local anaesthetic drugs
  • Bleeding tendency or with evidence of coagulopathy
  • Pre-existing respiratory disease
  • Neurological deficit or neuromuscular disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Single procedure on the day of surgery

Participants receive either a Selective Trunk Block (SeTB) or Supraclavicular Brachial Plexus Block (SC BPB) as anesthesia for upper extremity surgery.

1 procedure visit (in-person)

Trial Site Locations

Total: 1 location

1

Department of Anaesthesia & Intensive Care, Prince of Wales Hospital, Shatin, New Territories,

Hong Kong, Hong Kong

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Research Team

H

Hoi Ling Wong, RN, BN

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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