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To find out which guiding modality during regional Anaesthesi(axillary nerve block)causes the patient to get early loss sensation,inability to move,patients satisfaction,failure rate,adverse effect Comparison between ultrasound(newer modality)and peripheral nerve stimulation(older modality)

TO COMPARE ULTRASOUND AND PERIPHERAL NERVE STIMULATION GUIDANCE IN AXILLARY BRACHIAL PLEXUS BLOCK: A RANDOMISED CONTROL TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022534
Enrollment
60
Registered
2019-12-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Ultrasound guidance in giving axillary brachial plexus block: All patients in ultrasound groups will be given local anaesthetic using ultrasound and following parameters will be measure

Sponsors

Dheebak Raj
Lead Sponsor
DR MATHEWS JACOB
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All patients greater than or at 18 years of age and less than or at 85 years in American Society of Anaesthesiologists Physical Status Grade I-III undergoing day care surgical procedures in the tertiary hospital who have consented to the study will be included.

Exclusion criteria

Exclusion criteria: Exclusion Criteria Details Exclusion criteria will be patients who had history of local anaesthetic allergy, local infection, significant neuropsychiatric disorder, peripheral neuropathy and coagulopathy.

Design outcomes

Primary

MeasureTime frame
The difference in outcome between ultrasound and peripheral nerve stimulation guidance in terms of sensory and motor block onset timeTimepoint: All patient for 18 months period—

Secondary

MeasureTime frame
The difference in outcome between ultrasound and peripheral nerve stimulation guidance in terms block performing time, quality of block, local anaesthetic side effect, patient satisfaction ratio and failure rate.Timepoint: All patients for 18 months period—

Countries

India

Contacts

Public ContactDheebak Raj

ARMED FORCES MEDICAL COLLEGE

docmathewsjacob@gmail.com9049498131

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026