Viewing Study NCT06381752



Ignite Creation Date: 2024-05-06 @ 8:27 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06381752
Status: COMPLETED
Last Update Posted: 2024-04-24
First Post: 2024-04-05

Brief Title: Value of Continuous Passive Motion in Rehabilitation After Total Knee Replacement
Sponsor: Johannes Gutenberg University Mainz
Organization: Johannes Gutenberg University Mainz

Study Overview

Official Title: Value of Continuous Passive Motion in Rehabilitation After Total Knee Replacement - A Prospective Randomized Controlled Multicenter Trial
Status: COMPLETED
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Immediate rehabilitation after total knee arthroplasty TKA differs in terms of volume intensity but also type of treatment Continuous passive motion after TKA is so far only investigated for replacing physiotherapy This study is conducted to investigate CPM when it partially replaces group physiotherapy in terms of functional and patient-reported outcomes
Detailed Description: The aim of this study is to analyze the value knee function pain and quality of life of continuous passive motion CPM after total knee replacement TKR when it partially replaces group physiotherapy PT in inpatient rehabilitation to save human resources Patients are randomized to CPM group consisting of 3 daily sessions of 20 minutes each or to group PT consisting of 25 minutes physiotherapy in groups 5 days weekly Multimodal rehabilitation does not differ for both groups throughout the 3-week rehabilitation stay

Primary outcome is the Staffelstein Score German standard score in rehabilitation Secondary outcomes are Oxford Knee Score OKS active and passive range of motion ROM and pain on visual analogue scale VAS Return to work is assessed by post-operative days

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None