Single use negative pressure wound therapy system (Prevena ™) compared to standard wound care after spinal surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00021494

Enrollment

302

Registered

2020-10-05

Start date

2020-06-25

Completion date

Unknown

Last updated

2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

T81.4

Interventions

Group 1: Patients in the intervention group are treated with the Prevena wound therapy system after a WS operation. The Prevena™ Incision Management System is a single use negative pressure wound the-

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Spinal surgery in the BWS/LWS area from dorsal - Male and female patients over 18 years of age

Exclusion criteria

Exclusion criteria: - Known diseases that lead to an immune deficiency (HIV, leukemia) - Cortisone therapy - Radiotherapy - Chemotherapy

Design outcomes

Primary

Measure	Time frame
The aim of the study is to evaluate a possible influence on wound healing disorders in obese patients. The primary endpoint is the revision rate after 4 weeks using Fisher's exact test.	—

Secondary

Measure	Time frame
The secondary endpoint is logistic regression.	—

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement

yvonne.noll@diakovere.de0511-5354-649

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026