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LiquiBand Versus Dermabond Versus Sutures for Closure of Surgical Wounds

NCT01835405 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2017-01-24

No results posted yet for this study

Summary

To evaluate the cosmetic outcome, effectiveness, user and subject satisfaction, and safety of LiquiBand® Flex in relation to DermaBond Advanced™ and conventional sutures for the topical closure of surgical wounds.

Conditions

  • Surgical Incisions

Interventions

DEVICE

LiquiBand Flex

DEVICE

Dermabond Advanced

DEVICE

Sutures (Prolene)

Sponsors & Collaborators

  • Advanced Medical Solutions Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-20
Primary Completion
2014-02-14
Completion
2014-02-14

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 NCT01835405 on ClinicalTrials.gov