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A Post-Market Study of BandGrip in Traumatic Wound Closure Compared to Suture

NCT03628690 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2019-07-10

No results posted yet for this study

Summary

an unbalanced (2:1) randomized study comparing two methods of traumatic skin closure in an ER setting: BandGrip vs suture

Conditions

  • Laceration of Skin

Interventions

DEVICE

BandGrip

Topical skin closure device

DEVICE

Suture

Wound closure

Sponsors & Collaborators

  • BandGrip

    lead INDUSTRY

Principal Investigators

  • Dennis Donohoe · BandGrip

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-15
Primary Completion
2019-12-31
Completion
2020-02-29
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03628690 on ClinicalTrials.gov