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Comparative analysis in patients with Epidural Analgesia vs Ultrasound Guided Adductor Canal Block for better postoperative pain relief in total knee replacement surgery

Comparative Study Between Continuous Epidural Analgesia And Ultrasound Guided Continuous Adductor Canal Block For Postoperative Pain Management After Total Knee Replacement Surgery. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074519
Enrollment
114
Registered
2024-09-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: M808- Other osteoporosis with current pathological fracture

Interventions

Intervention1: Adductor canal block: With complete aseptic precautions , using a portable sonosite ultrasound system, the linear probe will be placed vertically to the thigh, midway between the anteri

Sponsors

Dr. Raghul Ramesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient in the age group of 18 to 60 years of both the sex. American society of anaesthesiologists {ASA} classifications 1 to 2 and scheduled for elective total knee replacement surgery.

Exclusion criteria

Exclusion criteria: Patient not willing for surgery Patient with coagulopathy Patient with infection at site of intervention Patient who are hypersensitive to the study drugs Patient undergoing bilateral TKA Patient with chronic narcotic use Patient with neuromuscular disease Patient refusal for surgery

Design outcomes

Primary

MeasureTime frame
Visual analogue scoreTimepoint: At 0,1,6,12,24,36 and 48 hours

Secondary

MeasureTime frame
Nausea, vomiting and Hemodynamic parameters (mean blood pressure, heart rate, spo2) and side effects such as pruritis, nausea, vomiting and requirement of analgesic doses. Rescue analgesic- 3mg morphine if given as a rescue dose if VAS more than 3 after 5ml of topup dose was given.Timepoint: 48 hours

Countries

India

Contacts

Public ContactRaghul Ramesh

Sri Balaji Vidyapeeth University

dilipko@gmail.com9094940243

Outcome results

None listed

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