Trials / Completed
CompletedNCT05095935
Medtronic Signia SDR Product Surveillance Registry
Medtronic Signia Small Diameter Reload Product Surveillance Registry
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 430 (actual)
- Sponsor
- Medtronic · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | N/A observational registry | N/A observational registry |
Timeline
- Start date
- 2021-08-10
- Primary completion
- 2024-10-01
- Completion
- 2024-10-01
- First posted
- 2021-10-27
- Last updated
- 2026-01-07
- Results posted
- 2026-01-07
Locations
14 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05095935. Inclusion in this directory is not an endorsement.