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Zip Arthroplasty Patient Satisfaction Evaluation

NCT03178266 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 41

Last updated 2019-05-15

Study results available
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Summary

This study is a prospective, randomized, single center, study to evaluate Zip Closure Device in subjects undergoing knee arthroplasty. Patients identified as candidates for knee arthroplasty and meet the study selection criteria will be approached and considered for the study. Knee Arthroplasty of 40 subjects will be enrolled where 20 subjects will receive ZipLine and 20 subjects will receive Staples.

Conditions

  • Knee Arthroplasty

Interventions

DEVICE

Knee Arthroplasty

Standard Knee Arthroplasty will be performed on study subjects. The closure method will be studied at 3 weeks and 6 weeks and patients will be asked about satisfaction with the closure method assigned.

Sponsors & Collaborators

  • ZipLine Medical Inc.

    lead INDUSTRY

Principal Investigators

  • Bruce Menkowitz, MD · Cheif of Surgery and Orthopaedics

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-12-01
Primary Completion
2018-05-01
Completion
2018-05-01

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 NCT03178266 on ClinicalTrials.gov