CompletedPhase 4

Prevena Spine for Use in Spine Surgery

United States104 participantsStarted 2022-12-01

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Patients undergoing spinal fusion surgery
✓. Over 18 years old

Exclusion criteria

✕. 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 judgment of the Investigator, would make the subject inappropriate for entry into this study
✕. Subjects who are pregnant at the date of surgery (SOC for surgery)

What they're measuring

Frequency of Surgical site infections

Timeframe: 1-6 weeks following surgery

Frequency of Wound dehiscence

Timeframe: 1-6 weeks following surgery

Frequency of Seroma

Timeframe: 1-6 weeks following surgery

Trial details

NCT IDNCT05555355

SponsorNorthwestern University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-11-01

View on ClinicalTrials.gov More Surgery trials