Ultrasound-Guided Supraclavicular Block With vs Without PNS

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorAga Khan University

About this trial

Peripheral Nerve Blockade (PNB) became reliable with the advent of Ultrasound (US) and Peripheral Nerve Stimulation (PNS).

US offers real-time visualization but has limitations, especially with deep or obscured nerves.

PNS complements US by confirming nerve proximity through motor responses. Combining both may enhance safety and success of nerve blocks. This study compares US-guided blocks with and without PNS in a randomized trial.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 18 years and older

ASA physical status I to IV

No contraindications to regional anaesthesia

Operative site located at the mid to lower arm, including the elbow, forearm, wrist, or hand

Disqualifiers

Patient's refusal to participate.

Inability to provide first-party consent due to cognitive impairment.

Cognitive dysfunction which can lead to difficulties in communication and cooperation of patient.

Preexisting neuropathy.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Peripheral nerve stimulator

    Device

    Peripheral nerve stimulator along with ultrasound

  • No peripheral nerve stimulator

    Device

    No peripheral nerve stimulator with ultrasound. Only ultrasound will be used

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: Ultrasound (US)Active comparator 1 intervention
Group B: Ultrasound+PNSExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Success rate of peripheral nerve block (PNB) with ultrasound-guided regional anesthesia (UGRA) with and without peripheral nerve stimulation (PNS)

Comparison of PNB success rate between UGRA alone and UGRA combined with PNS guidance.

Time frame
From administration of peripheral nerve block (PNB) until confirmation of successful block onset, assessed up to 60 minutes post-procedure

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: