Vashe Solution for Venous Ulcers

CT
OT
Overseen ByOlivier TACCA, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Laboratoires URGO
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

Evaluation of the efficacy (reduction of inflammatory signs suggesting a local infection) and tolerance (emergence and nature of adverse event) of Vashe solution vs Saline solution in the treatment of venous or mixed leg ulcers presenting inflammatory signs suggesting heavy bacterial load

Are You a Good Fit for This Trial?

Inclusion Criteria

My leg ulcer shows at least three signs of inflammation.
I have used compression therapy before and agree to use a two-layer system during treatment.
I have a leg ulcer mainly caused by vein problems.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either Vashe solution or Saline solution for wound irrigation

4 weeks
Weekly visits for treatment assessment

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Saline solution
  • Vashe solution

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Vashe solutionExperimental Treatment1 Intervention
Group II: Saline solutionActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Laboratoires URGO

Lead Sponsor

Trials
16
Recruited
3,000+