Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
ID06182059

Enhanced Recovery After Surgery and Total Knee Replacement: A Prospective, Randomized Study on the Role of Peripheral Nerve Blocks on Persistent Postoperative Pain Six Months After Surgery

Led by Policlinico di Monza SpA · Updated on 2025-06-03

436

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research evaluates pain management approaches in patients undergoing primary total knee replacement surgery. It compares two regional anesthesia techniques to see if one method reduces persistent postoperative pain six months after surgery. The trial is randomized and sponsored by Policlinico di Monza SpA, focusing on improving recovery and pain outcomes after knee arthropathy surgery. Participants receive either a continuous adductor canal block plus an ipack block or a continuous femoral nerve block combined with a continuous sciatic nerve block immediately after surgery. Both groups are given additional pain relief medications including paracetamol, ketorolac, dexamethasone, and morphine as needed. These interventions are aimed at assessing differences in pain control effectiveness over time. During the study, patients are monitored for persistent post surgical pain up to six months after surgery. Researchers also measure acute pain and morphine use during the first 72 hours post operation. The trial includes assessments of pain levels and medication requirements to track recovery progress. The total duration of participation extends through these follow-up periods to evaluate long-term pain outcomes and treatment impact.

CONDITIONS

Brief Title

Persistent Post Surgical Pain After Total Knee Arthroplasty

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary total knee replacement
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Allergy to local anesthetics or any drugs involved in the study
  • Contraindication to regional anesthesia
  • Chronic use of opioids
  • BMI over 35 kg/m2

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 72 hours

Participants undergo total knee replacement surgery with spinal anesthesia and receive either a continuous adductor canal block plus an ipack block or a continuous femoral nerve block plus a continuous sciatic nerve block. Multimodal analgesia is provided during this period.

Continuous monitoring during hospital stay post-surgery

Post-operative Follow-up

Duration - 6 months

Participants are followed to assess persistent post surgical pain and recovery progress after surgery.

Follow-up visits at intervals over 6 months

Trial Site Locations

Total: 1 location

1

Policlinico di Monza SPA

Monza, Monza Brianza, Italy, 20900

Actively Recruiting

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Research Team

G

Gianluca Cappelleri, MD

G

Gianluca Perseghin, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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