Single use negative pressure wound therapy system (Prevena ™) compared to standard wound care after spinal surgery
Not Applicable
Recruiting
- Conditions
- T81.4Infection following a procedure, not elsewhere classified
- Registration Number
- DRKS00021494
- Lead Sponsor
- Medizinische Hochschule Hannover
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 302
Inclusion Criteria
Spinal surgery in the BWS/LWS area from dorsal
- Male and female patients over 18 years of age
Exclusion Criteria
- Known diseases that lead to an immune deficiency (HIV, leukemia)
- Cortisone therapy
- Radiotherapy
- Chemotherapy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method The secondary endpoint is logistic regression.