To study the Minimum Effective Dose required to block the Selective truncal brachial plexus for elbow and forearm surgeries.

Selective truncal injection brachial plexus block for elbow and forearm surgeries- A dose finding study. - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091506

Enrollment

Registered

2025-07-23

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

Health Condition 1: S50-S59- Injuries to the elbow and forearm

Interventions

Intervention1: SELECTIVE TRUNCAL INJECTION BRACHIAL PLEXUS BLOCK FOR ELBOW AND FOREARM SURGERIES- A DOSE FINDING STUDY: In this study, Under USG guidance block is performed using the drug 0.5% bupiv

Eligibility

Inclusion criteria

Inclusion criteria: 1 Adult patients aged between 18 and 65 years 2 Scheduled for elective upper limb surgery requiring brachial plexus block 3 Classified as American Society of Anesthesiologists (ASA) physical status I to III 4 Willing and able to provide written informed consent 5 Cooperative and able to communicate effectively during the procedure

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Success rate of Surgical Block MEV90 estimationTimepoint: Block is assessed every 5 minutes till 40 min 0min 5 min 10 min 15 min 20 min 25 min 30 min 35 min 40 min	—

Secondary

Measure	Time frame
Sensory block onset time Motor Block Onset Time Duration of sensory and motor block Patient satisfaction scoreTimepoint: It is assessed for 40min after block and before incision	—

Countries

India

Contacts

Public ContactDr P Madhushree

Ballari institute of Medical Sciences and Research centre

nkiranchand@yahoo.com9845857056

Outcome results

None listed

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