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Comparison of adductor canal block in addition to epidural infusion versus continuous epidural infusion on post-operative pain in patients undergoing knee surgeries

Comparative study of adductor canal block in addition to epidural infusion versus continuous epidural infusion on post-operative analgesia in patients undergoing knee surgeries- A randomized control trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058674
Enrollment
70
Registered
2023-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: M236- Other spontaneous disruption of ligament(s) of knee

Interventions

Intervention1: Adductor canal block: Continuous epidural analgesia (CEA) is a common regional analgesia modality using the neuroaxial pathway for major orthopedic surgeries associated with decreased b

Sponsors

Bhagyalaxmi Chouhan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with ASA grade I, II and III undergoing total knee replacement surgery, meniscectomy, posterior cruciate ligament (PCL) repair and anterior cruciate ligament (ACL) repair with plan combining spinal epidural anaesthesia.

Exclusion criteria

Exclusion criteria: Patients with- Infected and bilateral TKA History of stroke Major neurological defect The chronic use of opioid or steroidal agents, Those with bleeding-coagulation disorder, Any spinal pathology that contraindicates neuraxial Blockade. Patients who refuse to give consent.

Design outcomes

Primary

MeasureTime frame
No or mild postoperative pain compared to combined epidural anaesthesiaTimepoint: Postoperatively immediately to 24 hours

Secondary

MeasureTime frame
post operative no painTimepoint: 24 hours postoperative period

Countries

India

Contacts

Public ContactBhagyalaxmi Chouhan

KAHER INSTITUTE

drrajeshmane@gmail.com9844131062

Outcome results

None listed

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