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A clinical trial to study efficacy of low dose interscalene and superficial cervical plexus block and superior trunk with supraclavicular nerve block in elective clavicular surgeries

Comparative study to evaluate clinical efficacy of low dose interscalene and superficial cervical plexus block with superior trunk and supraclavicular nerve block in adult patients undergoing elective clavicular surgeries- a prospective randomised double blinded study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039433
Enrollment
80
Registered
2022-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: S298- Other specified injuries of thorax

Interventions

Intervention1: INTERSCALENE BRACHIAL PLEXUS BLOCK: TWO APPROACHES OF BRACHIAL PLEXUS BLOCK THE INTERSCALENE WITH SUPERFICIAL CERVICAL PLEXUS BLOCK IS STUDIED FOR 15 mins Control Intervention1: SUPRACL

Sponsors

Pushti Alpeshkumar Majmundar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA-PS I AND II POSTED FOR CLAVICLE SURGERY BMI <35kg/m2

Exclusion criteria

Exclusion criteria: Patient not willing to consent for the procedure Local infection/open wound/ distorted anatomy in the affected side of the neck and supraclavicular area due to haematoma/ swelling. All respiratory/ pleural disease compromising respiration/ history of OSA Any indicators of difficult airway or history of difficult airway management Haemodynamic instability Allergic history to any local anaesthetics Coagulopathy Neuropathy Patients having undergone radiotherapy of neck region Pregnancy

Design outcomes

Primary

MeasureTime frame
To compare the feasibility of providing surgical anaesthesia as assessed by loss of pin prick sensation after 10 minutes with low dose (13ml) superior trunk block and supraclavicular nerve block with conventional interscalene brachial plexus block and superficial cervical plexus block in adult patients undergoing elective clavicular surgeriesTimepoint: every 30 minutes—

Secondary

MeasureTime frame
Onset and duration of motor blockageTimepoint: every 30 minutes;Onset and duration of sensory blockTimepoint: every 30 minutes;To assess hemidiaphragmatic paralysisTimepoint: begining of study and after block—

Countries

India

Contacts

Public ContactPushti Alpeshkumar Majmundar

JSS Medical College and Hospital

drsarikamshetty@yahoo.com

Outcome results

None listed

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