Effectiveness of Sorbion in the Treatment of Venous Leg Ulcers The Protocol Elements

University of Toledo Health Science Campus

Status: Terminated

Conditions: Venous Wound Ulcers

Treatments: Device: Sorbion Dressing

Study type: Interventional

Funder types: Other

Identifiers

NCT03020446

Sorbion Study

Details and patient eligibility

About

To follow the effectiveness of Sorbion Dressing in the treatment of highly exuding venous leg ulcers.

Full description

Wounds will be assessed for inclusion into the study, digital images of the wound will be taken, wound will be cleansed, a sorbion dressing will be placed on wound and a cover dressing with be used to keep in place. The wound will be assessed and a dressing change will take place weekly for 4 weeks. At the final visit a final wound evaluation will be done.

Enrollment: 3 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• venous leg ulcer

Exclusion criteria

• pregnant females

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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3 participants in 1 patient group

Sorbion dressing to venous leg ulcer

Experimental group

Description:

any venous leg ulcer will receive sorbion dressing weekly for 4 weeks than wound will be assessed

Treatment:

Device: Sorbion Dressing