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Analysis of contribution to pain relief after blocking specific nerves of the knee for patients undergoing knee replacement surgery

Contribution of targeted nerve blocks to postoperative analgesia in patients undergoing total knee replacement - A randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052336
Enrollment
120
Registered
2023-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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: Multiarm Randomized Controlled Trial: 4 groups Intervention2: GROUP B- ACB at the level of NVI WITH PCA: Group B- Adductor canal block (ACB) at the level of Nerve to Vastus Intermedius(

Sponsors

Internal- Fluid Research Grant
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1,2,3 Patients

Exclusion criteria

Exclusion criteria: ASA 4, Age less than 18 years, Deranged Coagulation Profile, Peripheral Neuropathy, Local Anaesthetic Allergy

Design outcomes

Primary

MeasureTime frame
To assess postoperative pain,Timepoint: To assess postoperative pain between the targeted nerve block groups on rest and on movement for 5 days,every 12 hourly for first 3 days,and 24 hourly for next 2 days—

Secondary

MeasureTime frame
Motor blockadeTimepoint: Assessment of motor function quadriceps femoris muscle for 5 days postoperatively—

Countries

India

Contacts

Public ContactLilly Sophia M

Christian Medical College

cmcrahulpillai@gmail.com9894460758

Outcome results

None listed

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