MedTrace Logo

Tourniquet on Total Knee Arthroplasty

NCT04923724 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 165

Last updated 2025-05-15

Study results available
· View outcomes & findings →

Summary

The purpose of this study is determine the effect on novel pressure-regulating tourniquet use on pain, functional recovery, sleep and total blood loss following total knee arthroplasty.

Conditions

  • Arthritis Knee

Interventions

DEVICE

tourniquet

tourniquet is a device used during total knee surgery.

DEVICE

No tourniquet

tourniquet is a device used during total knee surgery, this group does not get one

Sponsors & Collaborators

  • Zimmer Biomet

    collaborator INDUSTRY

  • Washington University School of Medicine

    lead OTHER

Principal Investigators

  • Robert Barrack · Washington University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-11-01
Primary Completion
2023-11-30
Completion
2024-11-27
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT04923724 on ClinicalTrials.gov