Medtronic Signia SDR Product Surveillance Registry

Status Recruiting

Clinical Trial Summary

The purpose of the registry is to confirm the safety and performance of the Signia™ Small Diameter Reload (SDR) when used in surgical procedures in a real-world setting in patients receiving surgery for indicated thoracic, abdominal, and pediatric applications, intraoperatively.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Minimally Invasive Surgical Procedures
Surgical Procedures, Operative

Clinical Trial Details

NCT number	NCT05095935
Study type	Observational [Patient Registry]
Source	Medtronic
Contact	PSR Study Team
Phone	1-800-633-8766
Email	rs.productsurveillanceregistry@medtronic.com
Status	Recruiting
Phase
Start date	August 10, 2021
Completion date	July 2025

View Details

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