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Evaluation of a 'Hand-Held' Fluorescence Digital Imaging Device for Real-Time Advanced Wound Care Monitoring (SMH/UHN)


N/A
18 Years
N/A
Not Enrolling
Both
Surgical Wounds, Abdominal Wounds

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Trial Information

Evaluation of a 'Hand-Held' Fluorescence Digital Imaging Device for Real-Time Advanced Wound Care Monitoring (SMH/UHN)


Inclusion Criteria:



1. > 18 years of age

2. males and females

3. receiving care as in-patient at St. Michael's Hospital

4. presenting with abdominal wounds resulting from general surgery with known or unknown
infection status.

Exclusion Criteria:

1. treatment with an investigational drug within 1 month before study enrolment

2. any contra-indication to routine wound care and/or monitoring

3. inability to consent

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Principal Investigator

Ralph S DaCosta, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University Health Network, Toronto

Authority:

Canada: Health Canada

Study ID:

12-5024-A

NCT ID:

NCT01650571

Start Date:

July 2012

Completion Date:

July 2013

Related Keywords:

  • Surgical Wounds
  • Abdominal Wounds

Name

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