Zip Arthroplasty Patient Satisfaction Evaluation

Completed

Conditions studied: Knee Arthroplasty

In brief

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.

Key facts

Study ID

NCT03178266

Run by

ZipLine Medical Inc.

People needed

41

Starts

2017-12-01

Expected to finish

2018-05-01

Last updated by the study team

2019-05-15

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients undergoing primary elective knee arthroplasty.
• Willing and able to provide informed consent and/or obtain legal guardian authorization
• Willing and able to comply with the subject-specific requirements outlined in the study protocol

You may not qualify if…

• Patients that do not meet the conditions listed in the wound closure device warnings, precautions, and contraindications (Appendix A)
• Patients with comorbidities or conditions that the investigator deems to be ineligible for the study
• Patients without the capacity to give informed consent (e.g., dementia)

Where it is running

• Montgomery Orthopaedics Associates — Norristown, Pennsylvania, United States

Full record on ClinicalTrials.gov

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