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comparison of negative pressure wound therapy between V.A.C and Renasys

comparison of negative pressure wound therapy between V.A.C and Renasys - comparison of negative pressure wound therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009283
Enrollment
6
Registered
2012-11-12
Start date
2012-11-12
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

burn and skin defect

Interventions

Each form of VAC and RENASYS is used to a half of wound region.

Sponsors

Plastic and reconstructive surgery, Osaka City University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient who obtained its consent for the competitive examination of the negative pressure wound therapy with a skin defect or a burn

Exclusion criteria

Exclusion criteria: 1. The patient with infection 2. The patient with necrosis tissue 3. The patient who has poor control of the bleeding 4. The patient having the allergic symptoms such as bronchial asthma, hives 5. In addition, the patient, judged the participation in this study to be inappropriate by the attending doctor

Design outcomes

Primary

MeasureTime frame
size, the condition of granulation, histology

Countries

Japan

Contacts

Public ContactTakaharu Hatano

Osaka City University Plastic and reconstructive surgery

hatano0321@yahoo.co.jp06-6645-3892

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026