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Perineural additives in ultrasound guided supraclavicular brachial plexus block

Comparative study of efficacy of addition of fentanyl and dexmedetomidine as adjuvants to 0.5% bupivacaine in ultrasound guided supraclavicular brachial plexus block-a prospective randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015438
Enrollment
90
Registered
2018-08-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients undergoing upper limb orthopaedic procedures

Interventions

Intervention1: Regional anaesthesia: Ultrasound-guided supraclavicular brachial plexus block Control Intervention1: 0.5% bupivacaine: Comparison of local anaesthetic 0.5% bupivacaine as control in com

Sponsors

BGS GLOBAL HOSPITALS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing unilateral upper limb surgeries of ASAI-II PS

Exclusion criteria

Exclusion criteria: Patient refusal Weight ,50 kg Infection at site of block Known hypersensitivity to drug Pregnants and lactating women

Design outcomes

Primary

MeasureTime frame
Duration of postoperative analgesiaTimepoint: In the postoperative period patients were assessed for pain and request for analgesic at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until administration of rescue analgesic—

Secondary

MeasureTime frame
Duration of motor blockTimepoint: In the postoperative period patients were assessed for motor power at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until recovery of full motor power;Duration of sensory blockTimepoint: In the postoperative period patients were assessed for sensation at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until resolution of block;SedationTimepoint: In the postoperative period patients were assessed for sedation at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until administration of rescue analgesic—

Countries

India

Contacts

Public ContactDrAbhay Prasad

BGS Global Hospital

drsantokrish@yahoo.co.in

Outcome results

None listed

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