Persistent Post Surgical Pain After Total Knee Arthroplasty

NCT ID
NCT06182059
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Policlinico di Monza SpA
Conditions
Knee Arthropathy

Overview

ClinicalTrials.gov lists this study as Recruiting.

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

Enrollment: 436 participants (Estimated).

What is being studied

  • Procedure: continuous peripheral nerve block

Who may be eligible

Ages
18 Years to 85 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * primary total knee replacement with a written informed consent Exclusion Criteria: * Allergy to local anesthetics or any drugs involve in the study * Controindication to regional anesthesia * chronic use of opioids * BMI \> 35 kg m2

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Italy

  • Monza Brianza, Italy: 1

Sample of listed locations

  • Policlinico di Monza SPA — Monza, Monza Brianza, 20900, Italy — Recruiting

Study details

Start date
January 12, 2024
Primary completion date
January 31, 2027
Completion date
July 31, 2027
First posted
December 26, 2023

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06182059
Registry last updated
September 21, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT06182059 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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