A Skin Stretching Wound Closure System

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2010 by Hillel Yaffe Medical Center.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier:
NCT01069614
First received: February 7, 2010
Last updated: February 16, 2010
Last verified: February 2010

February 7, 2010
February 16, 2010
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Not Provided
Safety and efficacy of wound closure [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01069614 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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A Skin Stretching Wound Closure System
Not Provided

A skin stretching device has been designed to stretch tissue prior to surgery, during surgery and in order to secure wounds following surgery. The device may be used in non-invasive and invasive applications.

Not Provided
Interventional
Phase 1
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Wounds
  • Injuries
Device: TopClosure 3S System
Experimental: Skin stretching device
Skin stretching device
Intervention: Device: TopClosure 3S System
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
30
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Inclusion Criteria:

  • Hard to close wounds

Exclusion Criteria:

  • Non-cooperative patients
Both
16 Years and older
No
Not Provided
Israel
 
NCT01069614
HYMC-09
Not Provided
Moris Topaz, MD, PhD, Hillel Yaffe Medical Center
Hillel Yaffe Medical Center
Not Provided
Not Provided
Hillel Yaffe Medical Center
February 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP