CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 41 enrolled
Drug / intervention
Knee Arthroplastydevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03178266
NCT03178266N/ACompleted

Zip Arthroplasty Patient Satisfaction Evaluation

ZipLine Medical Inc.·observational·Posted Jun 6, 2017·Updated May 15, 2019

In Brief

An observational study evaluating Knee Arthroplasty for Knee Arthroplasty. Completed, enrolled 41 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 6, 2017
Enrollment StartDec 1, 2017
Primary CompletionMay 1, 2018
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 9.1 years ago

Interventions

Knee Arthroplastydevice

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.