CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 430 enrolled
Drug / intervention
N/A observational registryother
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/NCT05095935
NCT05095935N/ACompleted
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Medtronic Signia Small Diameter Reload Product Surveillance Registry

Medtronic·observational·Posted Oct 27, 2021·Updated Jan 7, 2026

In Brief

An observational study evaluating N/A observational registry for Minimally Invasive Surgical Procedures and Surgical Procedures, Operative. Completed, enrolled 430 participants across 14 sites.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsMinimally Invasive Surgical Procedures, Surgical Procedures, Operative
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedOct 27, 2021
Enrollment StartAug 10, 2021
Primary CompletionOct 1, 2024
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 4.7 years ago

Interventions

N/A observational registryother

N/A observational registry