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NCT00013143 · ClinicalTrials.gov registry record · NA
Patient Profiling and Provider Feedback to Reduce Adverse Drug Events
A NA study of Adverse Drug Events, sponsored by US Department of Veterans Affairs.
- Completed
- Registry status
- NA
- Development phase
- 1,200
- Enrollment target
- 1
- Study location
NCT00013143 is a NA study of Adverse Drug Events that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 1,200 participants, above the 589-participant average among 6 other Adverse Drug Events trials with a reported enrollment target (104% higher). The trial reports 1 study location across 1 state.
The verdict
NCT00013143, a NA study of Adverse Drug Events, has completed, sponsored by US Department of Veterans Affairs.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,200 participants
- Enrollment target
- 1
- Study location
Study Summary
Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.
Conditions Studied
Interventions
- BEHAVIORAL Patient risk profiling (potential ADEs) w/provider feedback
Study Locations (1)
California
- VA Greater Los Angeles Healthcare System, West Los Angeles, CA - West Los Angeles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,200 participants |
| Start Date | 2001-06 |
| Est. Completion | 2003-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00013143
The ClinicalTrials.gov registry entry for NCT00013143 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,200 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 589-participant average among 6 other Adverse Drug Events trials with a reported enrollment target (104% higher). The listed sponsor is US Department of Veterans Affairs, which has 632 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Adverse Drug Events appearing as the primary indexed condition, and to 1 intervention - of which Patient risk profiling (potential ADEs) w/provider feedback is the first listed.
NCT00013143 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT00013143 about?
NCT00013143 is a clinical study titled "Patient Profiling and Provider Feedback to Reduce Adverse Drug Events". Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.
What is the current status of trial NCT00013143?
This trial is currently completed. It is a NA study. The enrollment target is 1,200 participants. The study started on 2001-06. Estimated completion is 2003-01.
What conditions does trial NCT00013143 study?
This clinical trial studies the following conditions: Adverse Drug Events.
What interventions are being tested in trial NCT00013143?
The interventions under investigation include: Patient risk profiling (potential ADEs) w/provider feedback (BEHAVIORAL).
Who is sponsoring clinical trial NCT00013143?
This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00013143 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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