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Clinical Trial Summary

The primary objectives for the registry is to evaluate the overall incidence of serious complications or adverse events for primary implants and replacement devices, and assess the cost and time efficiency for both physicians and patients. The Registry is a multi ASC data collection registry. Data collection will occur at the time of screening, implant, and 2 weeks after implant at the time of wound check.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03604133
Study type Observational [Patient Registry]
Source QuesGen Systems Inc
Contact Michael Jarrett, MBA
Phone 415-608-3570
Email mike.jarrett@quesgen.com
Status Recruiting
Phase
Start date August 24, 2017
Completion date August 24, 2028

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