Prospective, Randomized Study of 2 Different Wound Dressings

Launched by UNIVERSITY OF COLOGNE · Nov 13, 2013

Keywords

ClinConnect Summary

A monocentre, post CE-mark, randomized clinical trial will be conducted at the University of Cologne, Department of Orthopedics and Trauma Surgery.

Male or female subjects, 18 years and above, undergoing hip, knee or spinal surgery with an expected hospital stay for 4 days or more will be included in the trial. Individual trial duration will be for 7 days (follow-up).

Two hundred subjects will be included in the trial, i.e. 100 subjects per arm. The treatment arm (either new or standard wound dressing) will be assigned by randomization stratified by type of surgery (i.e. hip, knee or spin...

Gender

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Eligibility criteria

• Inclusion Criteria:
• • 1. Age ≥18years
• • 2. Have an expected total length of stay of 4 or more days
• • 3. Undergoing elective primary arthroplasty of the hip or knee or spinal surgery
• • 4. Undergoing hip surgery with a standard access
• • 5. Give their written informed consent to participate
• Exclusion Criteria:
• • 1. Dressing size does not fit the incision area
• • 2. Known allergy/hypersensitivity to any of the components of the dressing
• • 3. Multi-trauma
• • 4. Undergoing arthroplasty or spine surgery due to tumour or infection?
• • 5. Fractures
• • 6. Wound at the surgical site prior to surgery
• • 7. Neurological deficit of operated side (hemiplegia, etc.)
• • 8. Subject has documented skin disease at time of enrolment, as judged by the investigator