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Clinical Trials/ACTRN12605000180617
ACTRN12605000180617
Terminated
Phase 3

A Comparison of the effectiveness of daily Tenderwet dressings and QID normal Saline compress as wound debridement agents

Fremantle Hospital & Health Service0 sites60 target enrollmentAugust 19, 2005

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.

Registry
who.int
Start Date
August 19, 2005
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

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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