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Single Injection vs. Intermittent Bolus Infraclavicular Brachial plexus Block for Post-Operative Pain After Distal Humerus Surgery

Comparative Evaluation of Post-operative Analgesic Efficacy of single injection with adjuvant versus intermittent bolus technique in infraclavicular brachial plexus block in patients undergoing surgery below distal humerus: A Prospective randomized observer blinded study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083420
Enrollment
80
Registered
2025-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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: single injection of 0.5% bupivacaine,25ml with 4mg dexamethasone in Infra clavicular brachial plexus block: Total fentanyl consumption till 48 hours in post operative patients undergoin

Sponsors

SGPGIMS LUCKNOW
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient who will give written and informed consent Patient undergoing surgery below distal humerus. Patients belonging to ASA grade I and II.

Exclusion criteria

Exclusion criteria: Patient refusal. ASA grade III and IV BMI 35 kg/m2 Patient with polytrauma Patient who will have known allergy and intolerance to local anesthetics& having active skin infection. Patient with cognitive impairment, delirium, dementia and severe hearing loss Coexisting coagulopathy or anticoagulant or antiplatelet treatment that would be a contraindication to regional anesthesia. Patient having pre existing neurological deficit in forearm

Design outcomes

Primary

MeasureTime frame
Total fentanyl consumption in 48 hrs after surgery by use of IV Patient Controlled Analgesia Timepoint: 48 hours

Secondary

MeasureTime frame
Static & dynamic pain assessment by Mean NRS (Numeric Rating Scale)at 2hr,4hr,12hr,18hr,24hr,30hr,36hr,42hr & 48hr till 48 hrs Patient satisfactory score at 48hrs Quality of recovery score at 48hrs Total rescue analgesia used in 48 hrs Post operative nausea & vomitingTimepoint: 48 hours

Countries

India

Contacts

Public ContactDr Ganpat Prasad

Sanjay Gandhi Post graduate institute of medical sciences

rm126069@gmail.com9984921001

Outcome results

None listed

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