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NCT01854138 · ClinicalTrials.gov registry record · NA

Evaluating Advantages of Prevena After Hip and Knee Arthroplasty

A NA study of Infection of Total Hip Joint Prosthesis, sponsored by ProMedica Health System.

Completed
Registry status
NA
Development phase
248
Enrollment target
1
Study location

NCT01854138 is a NA study of Infection of Total Hip Joint Prosthesis that has completed, run by ProMedica Health System. The registered enrollment target is 248 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT01854138, a NA study of Infection of Total Hip Joint Prosthesis, has completed, sponsored by ProMedica Health System.

COMPLETED
Registry status
NA
Development phase
248 participants
Enrollment target
1
Study location

Study Summary

Determine the extent to which application of the Prevena vacuum system to clean surgical incisions immediately following surgical procedure (total hip or total knee arthroplasty) will reduce the rates of: * readmission to hospital for surgical intervention due to wound complications * seroma * hematoma * infection compared to group of patients whose wounds were covered with traditional gauze dressings.

Interventions

  • DEVICE Prevena Incision Management System

Study Locations (1)

Ohio

  • Wildwood Orthopaedic and Spine Hospital - Toledo

Trial Details

FieldValue
Enrollment Target 248 participants
Start Date 2014-01
Est. Completion 2015-04
Phase NA

Sponsor

ProMedica Health System

12 total trials

What the Registry Record Tells You About NCT01854138

The ClinicalTrials.gov registry entry for NCT01854138 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 248 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ProMedica Health System, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Infection of Total Hip Joint Prosthesis appearing as the primary indexed condition, and to 1 intervention - of which Prevena Incision Management System is the first listed.

NCT01854138 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT01854138 about?

NCT01854138 is a clinical study titled "Evaluating Advantages of Prevena After Hip and Knee Arthroplasty". Determine the extent to which application of the Prevena vacuum system to clean surgical incisions immediately following surgical procedure (total hip or total knee arthroplasty) will reduce the rates of: * readmission to hospital for surgical intervention due to wound complications * seroma * hema...

What is the current status of trial NCT01854138?

This trial is currently completed. It is a NA study. The enrollment target is 248 participants. The study started on 2014-01. Estimated completion is 2015-04.

What conditions does trial NCT01854138 study?

This clinical trial studies the following conditions: Infection of Total Hip Joint Prosthesis.

What interventions are being tested in trial NCT01854138?

The interventions under investigation include: Prevena Incision Management System (DEVICE).

Who is sponsoring clinical trial NCT01854138?

This trial is sponsored by ProMedica Health System, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01854138 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.