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NCT03830515

Evaluation of microMend Device to Close Lacerations

Status unknown NA Last updated 5 February 2019
What this trial tests

NA trial testing microMend in Lacerations in 30 participants. Status unknown.

Timeline
20 April 2018
Primary endpoint
31 October 2019
31 December 2019

Quick facts

Lead sponsorKitoTech Medical, Inc.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date20 April 2018
Primary completion31 October 2019
Estimated completion31 December 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

KitoTech Medical, Inc.

Who can join

Adults 18 to 75, any sex, with Lacerations or Wounds. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this study, total of 20 subjects will have lacerations will be closed with microMend, which is an FDA-listed wound closure product. microMend is a wound closure device that is the size and shape of a butterfly bandage and incorporates tiny Microstaples into an adhesive backing. Assessments by practitioners and Subjects of microMend will be made at Days 0 10, and 3 months using a combination of questionnaires and photographs.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Evaluation of microMend wound closure device in repairing skin lacerations.
    Nizami T, Beaudoin F, Suner S, Aluisio A, et al · · 2023 · PMID 37220958 · DOI 10.1136/emermed-2022-212667

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