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Clinical Trials/NCT01069614
NCT01069614UnknownPhase 1

A Skin Stretching Wound Closure System

Hillel Yaffe Medical Center2 sites in 1 country30 target enrollmentStarted: February 17, 2010Last updated:
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Conditions

Trial Snapshot

Phase
Phase 1
Enrollment
30
Locations
2
Primary Endpoint
Safety and efficacy of wound closure
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
16 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Hard to close wounds

Exclusion Criteria

  • •Non-cooperative patients

Outcomes

Primary Outcomes

Safety and efficacy of wound closure

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov

Study Sites (2)

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