A study to predict Successful regional block by non invasive method

A STUDY TO EVALUATE THE CHANGE IN PERFUSION INDEX AS AN INDICATOR OF EFFICIENT ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUS BLOCK IN PEDIATRIC PATIENTS - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/068881

Enrollment

Registered

2024-06-13

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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 Supra clavicular block: Outcome will be assessed at 0 minute 5 minute 10 minute 20 minute 30 minute Control Intervention1: nil: nil Control Intervention2: Inj. ROPIVACAINE 0.

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA Grade I and II Patients 2. Patient undergoing elective upper limb surgeries 3. Patient with informed consent

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Primary outcomes are that - Perfusion Index is expected to increase after supraclavicular brachial plexus block due to sympathetic blockade & vasodilation.Timepoint: Outcome will be assessed at 0 minute 5 minute 10 minute 20 minute 30 minute	—

Secondary

Measure	Time frame
To calculate any complication associated with the blockTimepoint: The secondary outcome will be assessed at 0 minute 5 minutes 10 minutes 20 minutes 30 minutes;to calculate the cut off value for PI for a successful Supraclavicular BlockTimepoint: The secondary outcome will be assessed at 0 minute 5 minutes 10 minutes 20 minutes 30 minutes	—

Countries

India

Contacts

Public ContactPraveen Petson

LLRM Medical College

dr_abhishek1979@rediffmail.com9927951681

Outcome results

None listed

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