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Comparison of Dexmedetomidine and dexamethasone in supraclavicular block for upper arm surgery

Comparison Between Dexamethasone And Dexmedetomidine As A Perineural Adjuvant In Supraclavicular Brachial Plexus Block - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098364
Enrollment
80
Registered
2025-12-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: Dexemethasone: Patient will receive Injection Dexamethasone 4mg diluted with Normal Saline upto 5ml with Injection 0.5 percent bupivacaine hydrochloride 15ml with inj lignocaine with ad

Sponsors

Peoples Hospital Bhanpur Bhopal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Weight 50-80 kilograms ASA grade I and II All patients scheduled for elective upper limb surgeries under supraclavicular brachial plexus block

Exclusion criteria

Exclusion criteria: Patient refusal for consent Age less than 18 years and more than 60 years ASA grade III and IV Patients with abnormal coagulation profile Patients with local skin site infections Patient allergic to study drugs Pregnant and lactating mothers Failure or inadaequate supraclavivular block patient will be excluded

Design outcomes

Primary

MeasureTime frame
To compare the effects of Dexmedetomidine and Dexamethasone as a perineural adjuvant to 0.5% Bupivacaine in supraclavicular brachial plexus block.Timepoint: UPTO 6 hours

Secondary

MeasureTime frame
To assess the onset time and duration of sensory and motor blockade of Dexmedetomidine with 0.5% Bupivacaine for Supraclavicular brachial plexus block. To assess the onset time and duration of sensory and motor blockade of Dexamethasone with 0.5% Bupivacaine for Supraclavicular brachial plexus block. To observe time required for Rescue Analgesia in both the groups. To compare the observations of the 2 groups. Timepoint: upto 6 hours

Countries

India

Contacts

Public ContactDr Akanksha Agarwal

Peoples College Of Medical Sciences and Research Centre Bhopal

akankshaagarwal2020@gmail.com8989147838

Outcome results

None listed

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