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Efficacy of MySkin Patch for the Healing of Cut Injuries and Abrasions

NCT01573234 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2014-01-13

No results posted yet for this study

Summary

Evaluation of clinical efficacy of My Skin (hydrogel and polyurethane film) plus best practice clinical care in subjects with cut injuries and abrasions with particular regard to: Wound healing (complete reepithelialization) and patient's pain.

In the context of the study will be collected secondary outcomes related to type of lesion and its clinical evolution through the analysis of the items in the scale of the Pressure Sore Status Tool(PSST).

Conditions

  • Wounds and Injuries
  • Abrasion
  • Cut Injuries

Interventions

DEVICE

MySkin patch

Hydrogel and polyurethane film

DEVICE

Gauze and Patch

Traditional Dressing

Sponsors & Collaborators

  • Artsana S.p.a.

    collaborator INDUSTRY

  • Associazione Infermieristica per lo studio delle Lesioni Cutanee

    lead OTHER

Principal Investigators

  • Tommaso Bianchi · Associazione Infermieristica per lo studio delle Lesioni Cutanee

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2013-12-31
Completion
2014-01-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01573234 on ClinicalTrials.gov