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A study where two adjuvent dexmedetomidine vs clonidine use with local anaesthetic agent in upper limb surgery.

A comparative study of dexmedetomidine vs clonidine as an adjuvent to local anaesthetic drug in supraclavicular brachial plexus block. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081088
Enrollment
60
Registered
2025-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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: Dexmedetomidine as an adjuvent to local anaesthetic 0.5mcg/kg: Dexmedetomidine as an adjuvent to local anaesthetic drug in supraclavicular brachial plexus block. Dose: 0.5mcg/kg Freque

Sponsors

Smt. Bhikiben Kanjibhai Shah Medical Institute and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient willing to sign inform consent. ASA grade I and II patients posted for elective upper limb surgeries under Supraclavicular Brachial Plexus Block

Exclusion criteria

Exclusion criteria: Patient refusal Infection at local site Hypersensitivity or Allergy to local anaesthetic agent Coagulation disorders Patient on Anticoagulants Alcoholic or patient with drug abuse Patients receiving any drug that interact with our study drug Pre Existing Nerve injury Inadequate effect of nerve block or supplemented with other type of anaesthesia

Design outcomes

Primary

MeasureTime frame
This prospective and observational study will help us to compare the efficacy between Inj. Bupivacaine and Inj Clonidine vs Inj Bupivacaine and Inj dexmedetomidine Improving the duration and Quality of analgesiaTimepoint: reversal of sensory and motor blockage and VAS score after giving blockage at following time point: 0 min 30 min 1 hr 2 hr 3 hr 4 hr 5 hr 7 hr 10 hr

Secondary

MeasureTime frame
Analgesia and haemodynamic responses to anaesthesia by having better outcome in haemodynamicsTimepoint: At end of surgery up to 12 hrs after surgery

Countries

India

Contacts

Public ContactDr Nilesh Shah

Smt. Bhikiben Kanjibhai Shah Medical Institute and Research Centre

nileshshah730@gmail.com09512305508

Outcome results

None listed

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