Wound Dressings for Hidradenitis Suppurativa

University of Miami

Status: Completed

Conditions: Hidradenitis Suppurativa

Treatments: Device: Cutimed Sorbact Hydroactive B wound dressing; Device: Sorbion Sana multi-star wound dressing; Device: Cutimed Siltect wound dressing

Study type: Interventional

Funder types: Other

Identifiers

NCT04194541

20191046

Details and patient eligibility

About

The primary purpose of this research is to determine how the types of wound dressings affect quality of life for people with Hidradenitis Suppurativa (HS).

Enrollment: 28 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Men and women ≥18 years of age
• Diagnosed with Hidradenitis Suppurativa (all stages of disease) by Dermatologist
• Presence of at least one lesion with active drainage
• Willing and able to provide informed consent

Exclusion criteria

• Subjects younger than 18-years-old.
• Prisoners
• Pregnant or lactating women
• Adults unable to consent

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

28 participants in 1 patient group

Treatment Group

Experimental group

Description:

Participants will be provided a kit containing 3 dressings: Cutimed Sorbact Hydroactive B, Cutimed Siltec, and Sorbion Sana multi-star. Participant can use their dressing of choice and can change their dressings as needed for 6 consecutive weeks.

Treatment:

Device: Sorbion Sana multi-star wound dressing

Device: Cutimed Siltect wound dressing

Device: Cutimed Sorbact Hydroactive B wound dressing