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Cryocompression After Total Knee Arthroplasty

NCT05395273 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-08-28

No results posted yet for this study

Summary

The overall aim of this study is to evaluate the effectiveness of a cryocompression device after total knee arthroplasty (TKA) compared to standard therapy.

Conditions

  • Cryotherapy Effect

Interventions

DEVICE

Game Ready cryocompression

Cryotherapy on the coldest tolerable level and intermittend compression on the knee

Sponsors & Collaborators

  • University of Applied Sciences and Arts of Southern Switzerland

    lead OTHER

Principal Investigators

  • Ron Clijsen, PhD · University of Applied Sciences and Arts of Southern Switzerland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-05-10
Primary Completion
2023-08-28
Completion
2023-09-15

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05395273 on ClinicalTrials.gov