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A Study Comparing Two Local Anesthetic Techniques for Reducing Pain After Knee Replacement Surgery

Comparison Of Femoral Block Using 0.2 percent Ropivacaine And Adductor Canal Block Using 0.5 percent Ropivacaine For Post-Operative Analgesia In Total Knee Replacement Surgeries- A Prospective Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097126
Enrollment
72
Registered
2025-11-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Nil: Nil Control Intervention1: Femoral Nerve Block: 15 ml of 0.5% Ropivacaine with 10ml of 2% Lignocaine with Adrenaline plus 4mg Dexamethasone given under USG guidance perineurally im

Sponsors

K S Hegde Medical Academy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing unilateral total knee replacement 2. American Society of Anaesthesiologists Physical status 1 to 3 3. BMI between18-35kg/m2

Exclusion criteria

Exclusion criteria: 1. Patients with [re-existing neurological deficits 2. Patients with lower limb surgery in past one year 3. Patients with regular consumption of strong opioids and steroids 4.Patients with allergy to Ropivacaine, Lignocaine

Design outcomes

Primary

MeasureTime frame
Pain scores using Visual Analogue Scores at rest and on movement at knee jointTimepoint: At baseline, 0 hours, 6 hours, 24 hours, 48 hours, 120 hours

Secondary

MeasureTime frame
Range of motion at knee joint and walking distanceTimepoint: At 24 hours, 48 hours, 120 hours;First instance of rescue analgesic and total cumulative dose of rescue analgesicsTimepoint: At 120 hours

Countries

India

Contacts

Public ContactDr Naik Amey Subhash

K S Hegde Medical Academy

anandabangera@gmail.com9845278880

Outcome results

None listed

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