Clinical Investigation of Two Different Wound Dressings

Status Terminated

Clinical Trial Summary

The primary objective of this investigation is to evaluate changes on Peri-Wound skin from baseline to termination when using two different wound dressings The secondary objectives are to evaluate pain before, during, and after dressing removal from baseline to termination

Clinical Trial Description

A prospective randomized clinical investigation will be conducted at two sites in Sweden. Male or female, 18 years or older with following wound types: - traumatic, surgical or dehisced wounds, - venous leg ulcer or pressure ulcer will be included into the clinical investigation. 32 evaluated subjects (i:e 16 subjects per arm) will be followed during maximum three weeks. The treatment arm (either silicon adhesive dressing or acrylic adhesive dressing). Patients will be randomized using optimal allocation (minimization) balancing for the following baseline variables type of skin (normal/dry/flaky/oily/moist) and age. Eligible patients will be randomized to receive either silicon adhesive dressing or acrylic adhesive dressing in a ratio of 1:1 provided. ;

Study Design

Related Conditions & MeSH terms

Wounds and Injuries

Clinical Trial Details

NCT number	NCT02904200
Study type	Interventional
Source	Molnlycke Health Care AB
Contact
Status	Terminated
Phase	N/A
Start date	October 2016
Completion date	May 2017

View Details

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