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NCT01843426 · ClinicalTrials.gov registry record · NA
Aortic Stenosis Pre-Transcatheter Aortic Valve Replacement (TAVR) Procedure CT Scan
A NA study, sponsored by Medical University of South Carolina.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT01843426 is a NA study that has completed, run by Medical University of South Carolina. The registered enrollment target is 40 participants.
The verdict
NCT01843426, a NA study, has completed, sponsored by Medical University of South Carolina.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate contrast media volume, safety and 30-day outcome of patients after a computed tomography (CT) scan. The results of this study will help to determine the minimum volume of contrast material that can be used to ensure patient safety while not compromising diagnostic image quality in high-risk patients.
Interventions
- DRUG Low-volume, low-concentration contrast (iodixanol - Visipaque 270) CT scan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2013-02 |
| Est. Completion | 2017-09-25 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01843426
The ClinicalTrials.gov registry entry for NCT01843426 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical University of South Carolina, which has 755 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Low-volume, low-concentration contrast (iodixanol - Visipaque 270) CT scan is the first listed.
NCT01843426 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01843426 about?
NCT01843426 is a clinical study titled "Aortic Stenosis Pre-Transcatheter Aortic Valve Replacement (TAVR) Procedure CT Scan". The purpose of this study is to evaluate contrast media volume, safety and 30-day outcome of patients after a computed tomography (CT) scan. The results of this study will help to determine the minimum volume of contrast material that can be used to ensure patient safety while not compromising diagn...
What is the current status of trial NCT01843426?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2013-02. Estimated completion is 2017-09-25.
What interventions are being tested in trial NCT01843426?
The interventions under investigation include: Low-volume, low-concentration contrast (iodixanol - Visipaque 270) CT scan (DRUG).
Who is sponsoring clinical trial NCT01843426?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
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