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Adding new Ultrasound guided blocks help in reducing pain after knee replacement surgeries

comparison of analgesic efficacy of ultrasound guided genicular nerve block in combination with femoral nerve block in Primary total knee Arthroplasty - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/02/063280
Enrollment
60
Registered
2024-02-29
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: 0.25% bupivacaine 5ml at each genicular nerve (superomedial superolateral and inferomedial genicular nerves)and 8mg dexamethasone: Group I(genicular nerve blocks+ Adductor canal block)

Sponsors

Sparsh Hospital Foundation
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Unilateral primary TKA

Exclusion criteria

Exclusion criteria: Poorly Controlled DM(Hba1c >8) Cirrhosis Chronic Renal Failure Stroke , Uncontrolled Epilepsy History Of Post Op Delirium History Of DVT (Therapeutic Use Of Anti-Coagulants) Chronic Alcoholism Chronic Smoker (1 Pack/Day Past Six Months) History of allergy to local anaesthetics. Cardiopulmonary Disease (Recent MI,S/P Cardio Thoracic Surgery, severe pulmonary artery hypertension,Arrythmias, ejection fraction

Design outcomes

Primary

MeasureTime frame
To compare the effect of addition of ultrasound guided genicular nerve block to anaesthetic techniques on postoperative pain in patients undergoing total knee replacement. Timepoint: To compare the effect of addition of ultrasound guided genicular nerve block to anaesthetic techniques on postoperative pain in patients undergoing total knee replacement. Pain will be assessed at 6 12 18 24 & 48 hourly postoperatively by an anesthesiologist

Secondary

MeasureTime frame
To compare the effect of addition of ultrasound guided genicular nerve blocks in patients undergoing total knee replacement on postoperative opioid requirement , ambulation & physiotherapyTimepoint: Post operative opioid consumption will be recorded during 0-6 hours, 6-12 hours,12-24 hours & 24-48 hours. Ambulation distance was measured in feet on day 0, day 1, day 2 and day 3. Proportion of patients receiving rescue analgesia in both groups will also be compared. Presence of motor weakness of quadriceps if any will be noted.

Countries

India

Contacts

Public ContactSoujanya

Sparsh Super Specialty Hospital

madonastephen25@gmail.com9606197707

Outcome results

None listed

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