Evaluation of Adhesion Properties in Wound Care Devices
NCT06392165 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2024-04-30
Summary
Molnlycke manufactures and markets self-adhesive wound care devices intended to protect various types of wounds during treatment. This study aims to measure and evaluate the adhesion properties of self-adhesive wound care devices. To measure the adhesion properties test strips will be applied to the participant's skin for a predetermined time and will be removed while measuring the adhesion properties afterwards. This method has been chosen since there is no in vitro method available that can simulate adhesion to human skin
Conditions
- Adhesion Properties of Wound Care Devices
Interventions
- OTHER
-
self-adhesive device
Test device which is self-adhesive
Sponsors & Collaborators
-
Molnlycke Health Care AB
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 67 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-04-24
- Primary Completion
- 2025-06-30
- Completion
- 2025-06-30
Countries
- Sweden
Study Locations
More Related Trials
-
A Case Series Evaluating a Collagen Wound Dressing to Treat Wounds
NCT03909503 ·Status: WITHDRAWN ·Phase: NA
-
A Dual-center Study Evaluating Clinical Acceptance of a NPWT Wound Care System
NCT04593693 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Use of EZCare/V1STA in the Management of Acute and Chronic Wounds
NCT00994162 ·Status: COMPLETED ·Phase: NA
-
Post Market Clinical Follow Up Study of Avance Foam Abdominal Dressing Kit in Open Abdomen
NCT01968811 ·Status: COMPLETED ·Phase: NA
-
Microlyte Dressing in the Management of Wounds
NCT03204851 ·Status: UNKNOWN ·Phase: NA
-
A Study to Evaluate the Benefits of Using a Range of Wound Care Products From a Single Manufacturer
NCT02937909 ·Status: TERMINATED ·Phase: NA
-
A Multi-centre Evaluation of the Performance of Window Dressings on Subjects With High Risk Pressure Ulceration
NCT01438541 ·Status: COMPLETED ·Phase: PHASE4
-
A Prospective, Open, Non-controlled Clinical Investigation to Evaluate a New Negative Pressure Wound Therapy (NPWT) System to be Used in the Treatment of Acute Non-infected Wounds and Post Surgical Infected Wounds
NCT01195896 ·Status: COMPLETED ·Phase: NA
-
Smart Bandage With Telemonitoring vs Standard Care for Venous Leg Ulcer: Randomized Trial
NCT07163195 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Clinical Study to Compare 3 Multi-Layered Foam Dressings for the Management of Chronic Wounds
NCT03662997 ·Status: COMPLETED ·Phase: NA
-
Proof of Concept (Design Validation) in Patient With Hard to Heal Wounds Such as Pressure Ulcer, Diabetic Foot Ulcer and Leg Ulcer, Leia
NCT01966380 ·Status: TERMINATED ·Phase: PHASE2
-
An Exploratory Research on the Efficacy and Safety of Antibacterial Absorbable Dressing in Chronic Non-healing Wounds
NCT07261501 ·Status: RECRUITING ·Phase: NA
-
A Comparison of an Investigational Dressing to Tegaderm Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
NCT01013792 ·Status: TERMINATED ·Phase: NA
-
Evaluation of Safety and Activity of Celaderm in Healing Venous Leg Ulcers
NCT00399308 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Investigation of the Clinical Performance of Biatain Fiber Ag on Venous Leg Ulcers
NCT05873257 ·Status: COMPLETED ·Phase: NA
-
A Prospective, Open, Non-controlled Clinical Investigation to Evaluate the Performance and Safety of an Antimicrobial Foam Transferring Dressing in Patients With Malignant Wounds
NCT02431741 ·Status: COMPLETED ·Phase: NA
-
TITLE: An Open, Non-comparative, Multi-centre Post Marketing Clinical Follow-up (PMCF) Investigation to Evaluate Performance and Safety on Diabetic Foot Ulcer, DFU, When Using Mepilex Transfer Ag as Intended
NCT01964521 ·Status: COMPLETED ·Phase: NA
-
Assessment of the Wound Healing Efficacy and Tolerance of a Medical Device on Wounds in Healthy Subjects.
NCT04687839 ·Status: COMPLETED ·Phase: NA
-
Randomized Controlled 8-week Crossover Evaluation of Compression Bandage Systems for Venous Leg Ulcers
NCT00301496 ·Status: COMPLETED ·Phase: NA
-
Open Multi-centre Investigation to Evaluate Signs and Symptoms of Local Inflammation/Infection on Chronic Ulcers and Partial Thickness Burns When Using Mepilex Border Ag as an Anti-microbial Wound Dressing
NCT01214811 ·Status: COMPLETED ·Phase: PHASE3
-
Prospective, Randomized, Non-inferiority Investigation to Compare Effects of Mepitel® One and UrgoTul® Dressings in Acute Wound Management (Only)"
NCT02237118 ·Status: COMPLETED ·Phase: NA
-
Evaluating the Efficacy of an Absorbent Foam Dressing Containing Silver (Mepilex Ag) Versus the Same Dressing Without Silver Used on Subjects With Venous Leg Ulcers or Mixed Ulcers
NCT01036438 ·Status: COMPLETED ·Phase: PHASE4
-
The Difference in Wound Size Reduction Comparing Two Frequently Used Wound Dressings in Everyday Care
NCT03596112 ·Status: COMPLETED ·Phase: NA
-
An Evaluation of a Fibrillar Collagen Dressing to Treat Chronic, Stalled Lower-extremity Wounds
NCT03723577 ·Status: WITHDRAWN ·Phase: NA
-
A Clinical Evaluation of a Honey Impregnated Dressing at Removing Necrotic Tissue From Chronic Wounds
NCT03412929 ·Status: TERMINATED ·Phase: NA