HidraWear Study for Hidradenitis Suppurativa Wounds
NCT04449354 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2024-10-21
Summary
The product, HidraWear AX (www.hidrawear.com) is and adhesive free wound dressing system for the every day home care of Hidradenitis Suppurativa (HS), a debilitating disease of the skin for which there are limited wound dressing products.
This is a study to assess the use HidraWear Ax vs current product and method of use, and to determine the impact on patients' quality of life.
Conditions
- Hidradenitis Suppurativa
- Hidradenitis
Interventions
- DEVICE
-
HidraWear Ax
An adhesive free wound dressing fixation device for people living with Hidradenitis Suppurativa (HS), Hidrawear AX, designed to make dressing changes quick and easy for subjects. The unique features of the product completely remove the use of adhesives on the skin.The body conforming garment acts as a second skin and incorporates largely perforated panels over wound affected areas, minimising skin contact and aerating the area. The main function of the perforated is to act as a retaining device for the wound pads. The garment facilitates easy insertion, removal, precise positioning and adjustment of a non- adhesive wound dressing onto the effected wound space. The perforated section of the garment sits on the outer surface of the dressing providing provisional fixation. Next, an outer patch is placed on the outside of the garment on the footprint of the dressing. Through a hook and loop mechanism the dressing is now fully secured in place.
Sponsors & Collaborators
-
HidraMed Solutions Ltd
lead INDUSTRY
Principal Investigators
-
Trevor Duffy · Hermitage Clinic
Study Design
- Allocation
- NA
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 99 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-10-30
- Primary Completion
- 2020-10-03
- Completion
- 2020-10-03
Countries
- Ireland
Study Locations
More Related Trials
-
Skin Manifestations Associated With Adhesives in Diabetes Technology Tools
NCT04853810 ·Status: COMPLETED
-
Drug Patch Tests in Patients With Severe Cutaneous Adverse Reaction to Drugs (SCARs)
NCT03176342 ·Status: UNKNOWN ·Phase: NA
-
An Evaluation of the Reduction in Erythema in Adult Patients With Moderate to Severe Persistent Facial Erythema Associated With Rosacea
NCT03352323 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluation of Tetrix Cream in the Healing of Injured Skin in Subjects With Contact Dermatitis
NCT00643214 ·Status: COMPLETED ·Phase: NA
-
Safety and Effectiveness of an Auricular Spray
NCT06085443 ·Status: COMPLETED ·Phase: NA
-
Novel Skin Care for Immunotherapy- Related Dermatologic Toxicities
NCT04929834 ·Status: UNKNOWN ·Phase: NA
-
Sensitization Study of ATx201 in Healthy Volunteers
NCT03375957 ·Status: COMPLETED ·Phase: PHASE1
-
Internet and Social Media Use in Dermatology Patients
NCT03913598 ·Status: COMPLETED
-
A 47 Hour Occlusive Cutaneous Skin Patch Test on Adult Subjects With Dry/Atopic Skin
NCT02620293 ·Status: COMPLETED ·Phase: PHASE1
-
Study About Effectiveness of Silver-Containing Textiles for Treatment of Acute Neurodermatitis
NCT00196430 ·Status: COMPLETED ·Phase: PHASE3
-
Evaluation of Irritancy/Allergic Sensitivity to Natural Personal-care Products by Patch Tests
NCT01816542 ·Status: UNKNOWN ·Phase: NA
-
Acceptance of Telemedicine in Dermatology Patients, Physicians and Medical Staff
NCT04495036 ·Status: COMPLETED
-
A Non-Drug Study Detecting And Quantifying Nocturnal Scratch Behaviors From Wrist Actigraphy Data In Adult Healthy Volunteers And Participants With Atopic Dermatitis (AD)
NCT04262791 ·Status: TERMINATED ·Phase: PHASE1
-
Pre-SunBeam TEWL AUC
NCT04226092 ·Status: COMPLETED ·Phase: NA
-
The Use of Medical Grade Honey in the Prevention of Bone Anchored Hearing Aid Associated Skin Breakdown
NCT03929224 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Evaluate Microneedle-based Collection of Dermal Interstitial Skin Fluid in Healthy Participants and Atopic Dermatitis Participants
NCT06934980 ·Status: COMPLETED
-
Birth Cohort: Development of IgE Autoantibodies in Newborns With (High Risk of) Atopic Dermatitis
NCT07316465 ·Status: RECRUITING ·Phase: NA
-
An Open Label, Safety Study to Assess the Potential for Adrenal Suppression.
NCT02932891 ·Status: COMPLETED ·Phase: PHASE2
-
A Double-Blind, Multiple Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 in Hereditary Angioedema Participants
NCT02093923 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Safety and Tolerability of AC-1101 Topical Gel in Patients with Granuloma Annulare
NCT05580042 ·Status: COMPLETED ·Phase: PHASE1
-
Development and Evaluation of an Artificial Intelligence Model for the Diagnosis of Aeroallergies
NCT05918354 ·Status: COMPLETED
-
Clinical Evaluation of Bacitracin
NCT00132600 ·Status: COMPLETED ·Phase: PHASE2
-
Skin Barrier Assessment in Pregnancy and at Birth
NCT04445298 ·Status: UNKNOWN
-
Safety Study of Gene-modified Autologous Fibroblasts in Recessive Dystrophic Epidermolysis Bullosa
NCT02493816 ·Status: COMPLETED ·Phase: PHASE1
-
Cooling Pillow for Atopic Dermatitis
NCT01132651 ·Status: COMPLETED ·Phase: NA