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A Skin Stretching Wound Closure System

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01069614
Enrollment
30
Registered
2010-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2010-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Injuries, Wounds

Keywords

Equipment and supplies

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.

Interventions

DEVICETopClosure 3S System

Sponsors

Hillel Yaffe Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hard to close wounds

Exclusion criteria

* Non-cooperative patients

Design outcomes

Primary

MeasureTime frame
Safety and efficacy of wound closure

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026