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NCT01137786 · ClinicalTrials.gov registry record · Phase 4
Kidney Damage in Patients With Normal eGFR
A Phase 4 study of Coronary Artery Stenosis, sponsored by Bracco Diagnostics.
- Completed
- Registry status
- Phase 4
- Development phase
- 49
- Enrollment target
- 1
- Study location
NCT01137786: Completed Phase 4 study of Coronary Artery Stenosis, sponsored by Bracco Diagnostics.
NCT01137786 is a Phase 4 study of Coronary Artery Stenosis that has completed, run by Bracco Diagnostics. The registered enrollment target is 49 participants, below the 1,654-participant average among 4 other Coronary Artery Stenosis trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01137786, a Phase 4 study of Coronary Artery Stenosis, has completed, sponsored by Bracco Diagnostics.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 49 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a pilot study, randomized, double-blind, parallel group comparison of two iodinated contrast agents used during percutaneous coronary intervention (PCI). All patients enrolled must have normal eGFR. Statistical summaries will be presented to analyse the various laboratory tests for the two groups.
Primary Outcome
Mean change from baseline values for serum NGAL at 2,4,6,24,48 and 72 hours, and urine NGAL at 2,4,6,24, and 48 hours following the administration of non-ionic low osmolar contrast media.
Conditions Studied
Interventions
- DRUG Non ionic contrast media comparator
Study Locations (1)
Illinois
- Prairie Cardiovascular Consultants, Ltd. - Springfield
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 49 participants |
| Start Date | 2010-12 |
| Est. Completion | 2012-04 |
| Phase | Phase 4 |
What the finished NCT01137786 record still lists
NCT01137786 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 1,654-participant average among 4 other Coronary Artery Stenosis trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Coronary Artery Stenosis appearing as the primary indexed condition, and to 1 intervention - of which Non ionic contrast media comparator is the first listed.
NCT01137786 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT01137786 about?
NCT01137786 is a clinical study titled "Kidney Damage in Patients With Normal eGFR". This is a pilot study, randomized, double-blind, parallel group comparison of two iodinated contrast agents used during percutaneous coronary intervention (PCI). All patients enrolled must have normal eGFR. Statistical summaries will be presented to analyse the various laboratory tests for the two g...
What is the current status of trial NCT01137786?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 49 participants. The study started on 2010-12. Estimated completion is 2012-04.
What conditions does trial NCT01137786 study?
This clinical trial studies the following conditions: Coronary Artery Stenosis.
What interventions are being tested in trial NCT01137786?
The interventions under investigation include: Non ionic contrast media comparator (DRUG).
Who is sponsoring clinical trial NCT01137786?
This trial is sponsored by Bracco Diagnostics, which has 37 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01137786 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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