ACTRN12605000180617
Terminated
Phase 3
A Comparison of the effectiveness of daily Tenderwet dressings and QID normal Saline compress as wound debridement agents
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Fremantle Hospital & Health Service
- Enrollment
- 60
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients with chronic, slow/non healing (defined as a wound that shows no progress towards healing in 4 weeks) venous or mixed leg ulcers.2\. Patients who are able to understand the purpose of the study and give informed consent.
Exclusion Criteria
- •1\.Patients with severe systemic infections;2\. Patients with arerial ulcers;3\. Patients with severe lymphoedema or excessive wound exudate;4\. Patients taking immunosuppressive drugs.
Outcomes
Primary Outcomes
Not specified
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