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Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks — RAFDT  

Inguinal Hernia Clinical Trial

Official title:
Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks

Clinical Trial Summary

A post-market clinical follow-up study for ReliaTack™ articulating reloadable fixation device with deep purchase tacks

Clinical Trial Description

A retrospective, multi-center, chart review of medical records on the use of the device for two (2) surgical procedure indications:

1. inguinal/femoral hernia

2. ventral hernia

A minimum of 4 sites in the United States will perform chart review and enter 116 study records in the database for data collection. The 116 subject records will be comprised of 76 for the inguinal/femoral indication, and 40 for the ventral indication. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03526341
Study type Observational
Source Medtronic - MITG
Contact
Status Completed
Phase
Start date April 25, 2018
Completion date September 10, 2019
View Details
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