Prevena Spine for Use in Spine Surgery

Description

A pilot, prospective, single-center study for the investigation of the use of Prevena Vacuum-Assisted Closure devices in patients undergoing spine surgery.

Conditions

Surgery, Incision, Surgical

Talk to us

Study Overview

On this page

Study Details

Study overview

A pilot, prospective, single-center study for the investigation of the use of Prevena Vacuum-Assisted Closure devices in patients undergoing spine surgery.

A Prospective, Single-center Study for the Investigation of the Use of Prevena Vacuum-Assisted Closure Devices in Patients Undergoing Spine Surgery

Prevena Spine for Use in Spine Surgery

Condition
Surgery
Intervention / Treatment

-

Contacts and Locations

Chicago

Northwestern Memorial Hospital, Chicago, Illinois, United States, 60611

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patients undergoing spine surgery that requires closure by plastic surgeon
  • 2. Over 18 years old
  • 3. Risk Score Cutoff 80+
  • 4. (Control) Matched to a prospective research participant
  • 1. Risk Score Cutoff \<80
  • 2. Medical or psychiatric condition that may increase the risk with study participation, may complicate patient compliance, or may interfere with the interpretation of study results and, in the judgement of the Investigator, would make the subject inappropriate for entry into this study
  • 3. Subjects who are pregnant at the date of surgery (SOC for surgery)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Northwestern University,

Study Record Dates

2024-10-01