Per-subject investigator report for procedure completion using the Investigational Device
| Group | Value | 95% CI |
|---|---|---|
| OEC Elite Imaging Arm | 11 |
Last reviewed · How we verify
Clinical Evaluation of the OEC Elite Vascular Mobile Fluoroscopy System
NA trial testing OEC Elite system in Interventional Vascular Conditions in 12 participants. Terminated before completion.
| Lead sponsor | GE Healthcare |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | other |
| Enrollment | 12 |
| Start date | 19 June 2017 |
| Primary completion | 7 July 2017 |
| Estimated completion | 7 July 2017 |
| Sites | 1 location across Canada |
GE Healthcare — full company profile →
Adults 18 to 75, any sex, with Interventional Vascular Conditions. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Per-subject investigator report for procedure completion using the Investigational Device
| Group | Value | 95% CI |
|---|---|---|
| OEC Elite Imaging Arm | 11 |
The total number of per subject survey completion reflecting the investigator opinion of procedures completed with the investigational device
| Group | Value | 95% CI |
|---|---|---|
| OEC Elite Imaging Arm | 11 |
The purpose of the study is to collect survey data on the use of the OEC Elite Mobile Fluoroscopy System based on the routine clinical use of the device.
No peer-reviewed publications indexed yet for this trial.
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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing