Regional Anaesthesia: Brachial Plexus Block for upper limb surgeries comparing two different concentration of the same drug in terms of onset of block, duration of block. Drug being Bupivacaine -A Controlled Study ?

Brachial Plexus Block: Comparative Study Of Bupivacaine High Concentration Low Volume Versus Bupivacaine Low Concentration High Volume -A Randomised Controlled Study ? - NIL

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065395

Enrollment

Registered

2024-04-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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: Brachial plexus block under ultrasound guidance: Brachial plexus block under ultrasound guidance for upper limb surgery comparing the onset of block, duration of block with drug bupivac

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either gender, aged between 18 to 65 years, posted for upper limb correction surgeries. Patients willing to participate in the study by obtaining the written informed consent

Exclusion criteria

Exclusion criteria: Age less than 18 or age more than 65, unwilling patient, uncooperative patients, patients allergic to bupivacaine

Design outcomes

Primary

Measure	Time frame
1.Duration of analgesia 2.Onset of blockade Timepoint: 1.Duration of analgesia at 30min, 1hour, 2hour, 3hour, 4hour or more than 4hour 2.Onset of blockade 5min, 10min, 15min, 20 min, 25min or 30min	—

Secondary

Measure	Time frame
1. Total dosage of rescue analgesics required in first 24h 2. Adverse effects if any 3. Intra operative and post operative haemodynamic parametersTimepoint: 24h	—

Countries

India

Contacts

Public ContactMaj Dr Varun Bapurao Parvatikar

Command Hospital Airforce Bangalore

vijaimn7@yahoo.com6005404546

Outcome results

None listed

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