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Study of Dexamethasone as an Adjuvant to Levobupivacaine for analgesic efficacy in Infraclavicular Brachial Plexus Block in patients undergoing Upper Limb Surgery

Study of Dexamethasone as an Adjuvant to Levobupivacaine for Analgesic efficacy in Infraclavicular Brachial Plexus Block in patients undergoing Upper Limb Surgery - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079126
Enrollment
60
Registered
2025-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified Health Condition 2: X92-Y09- Assault Health Condition 3: M96-M96- Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Perineural Levobupivacaine with Dexamethasone: To evaluate the duration of analgesia with perineural Levobupivacaine with Dexamethasone in Infraclavicular Brachial Plexus Block for uppe

Sponsors

Dr Sarvjeet Kaur
Lead Sponsor
Dr Mukesh Kumar
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with American Society of Anaesthesiologists grade I and II 2. Patients between age of 18-60 years, giving valid informed and written consent

Exclusion criteria

Exclusion criteria: 1. Patients with inability to comprehense pain 2. Patients who have allergy to study drugs 3. Patients with local site infections 4. Patients having coagulation abnormalities 5. Patients who are on prolonged analgesics

Design outcomes

Primary

MeasureTime frame
Duration of sensory and motor BlockTimepoint: Every 1 hr till it resolves

Secondary

MeasureTime frame
Quality of analgesiaTimepoint: Every 1 hr till it resolves

Countries

India

Contacts

Public ContactDr Sarvjeet Kaur

GGSMCH, Faridkot

drsarvjeetk@gmail.com9915680508

Outcome results

None listed

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