A COMPARATIVE STUDY OF ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUS BLOCK WITH OR WITHOUT PRESSURE MONITORING FOR UPPER LIMB SURGERIES TO ASSESS COMPLICATIONS RELATED TO PERIPHERAL NERVE BLOCK.

Prospective Randomised Comparative Study of Ultrasound Guided supraclavicular Brachial Plexus Block With Or Without Pressure Monitoring - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/108554

Enrollment

Registered

2026-04-16

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

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

Interventions

Intervention1: USG guided Supraclavicular brachial plexus block: 20ml of 0.5% Bupivacaine with 4mg Dexamethasone. Control Intervention1: Usg guided supraclavicular brachial plexus block with pressure

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged between 18 and 65 years 2. Patients scheduled for upper limb surgeries under supraclavicular brachial plexus block. 3. Individuals belonging to American Society of Anesthesiologists (ASA) physical status I or II 4. Patients willing to give informed written consent for the study.

Exclusion criteria

Exclusion criteria: 1. Patient refusal. 2. Patients with known hypersensitivity to the study drug. 3. Patient with coagulopathy. 4. Patients with a history of substance abuse, psychiatric illness. 5. Patient with infection at the injection site.

Design outcomes

Primary

Measure	Time frame
To assess, compare and evaluate onset, duration of nerve blockade in both the groups & impact of pressure monitoring on accuracy of needle placement and spread of local anaesthetics.Timepoint: Post Induction maternal haemodynamics ( HR, SBP,DBP,MAP,RR, SPO2) at 2min, 4min, 6min, 8min, 10min, 15min, 20min, 25min, 30min, 40min, 50min, 60min, 120mins,	—

Secondary

Measure	Time frame
To assess the complications related to peripheral nerve block.Timepoint: sensory loss , motor loss, pain , tingling,numbness , paraesthesia for 30mins,60mins,2hours,4hours,6hours, 8hours, 12hours ,16hours , 20hours,24hours,28hours ,32hours , 48hours,52hours , 62hours, 72hours .	—

Countries

India

Contacts

Public ContactDr Geetanjali S M

BGS GIMS

geetp11@gmail.com9739945846

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026