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Pain relief options after total Knee Replacement.

Comparison of Adductor canal block with local infiltration analgesia for post-operative pain management in total knee arthroplasty

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/07/035157
Enrollment
90
Registered
2021-07-27
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: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: ADDUCTOR CANAL BLOCK: USG guided adductor canal block given and dose is (Bupivacaine 0.125% + Dexmedetomidine 0.5mcg/kg) Control Intervention1: Local Infilitration Analgesia (LIA): LIA

Sponsors

DEPARTMENT OF ANAESTHESIOLOGY AND CRITICAL CAREJNMCHAMU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I and II patients of either sex 2. Age between 18-75 years. 3. Weight between 55 -100 kg

Exclusion criteria

Exclusion criteria: 1. Patients with mental dysfunction or cognitive deficiency. 2. Patients with neuro-muscular, vestibular, hepatic or major systemic disease. 3. History of psychiatric illness 4. History of alcohol or drug abuse 5. History of allergy to local anaesthetic 6. Medical conditions affecting balance and coordination 7. Patient who is not giving consent. 8. Neuropathies associated with disease condition, lesion, drugs etc

Design outcomes

Primary

MeasureTime frame
Primary Objective: Pain relief assessment as measuredd by - Numerical Rating Scale (NRS) score changesTimepoint: Time to 1st perception of pain (NRS3)

Secondary

MeasureTime frame
Secondary Objective: Time to 1st rescue analgesic requirement (NRS3) Rescue analgesia needed in 1st 24 hours. Overall patient satisfaction score. Associated complicationsTimepoint: 10 months

Countries

India

Contacts

Public ContactMOHD JAVED KHAN

jnmch amu aligarh

naziatauheed15@gmail.com7895330665

Outcome results

None listed

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