Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT03286179 · ClinicalTrials.gov registry record
Standardizing Emergency Work-ups Around Risk Data
A clinical trial, sponsored by Kaiser Permanente.
- Completed
- Registry status
- 13,419
- Enrollment target
NCT03286179: Completed study, sponsored by Kaiser Permanente.
NCT03286179 is a clinical trial that has completed, run by Kaiser Permanente. The registered enrollment target is 13,419 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03286179 has completed, sponsored by Kaiser Permanente.
- COMPLETED
- Registry status
- 13,419 participants
- Enrollment target
Study Summary
Chest pain is the second leading reason for emergency department (ED) visits in the United States. Resource utilization for this ED subpopulation is particularly high, in part due to a dearth of accepted standardized clinical approaches and general overestimation of risk on the part of both providers and patients. This prospective observational cohort study seeks to address this issue by providing externally validated risk scores for major adverse cardiac events using a web-based clinical decision support platform (RISTRA) embedded within the electronic health record at 13 Kaiser Permanente Northern California (KPNC) EDs over a 12-month period. The decision support will provide risk estimates specific to the KPNC patient population. This studies hypothesis is that the provision of more accurate risk estimation for major adverse cardiac events will improve informed decision making by both providers and patients, resulting in less provocative testing and lower ED lengths of stay amongst low risk patients, as well as improving medical management among non-low risk patients and decreasing future rates of major adverse cardiac events.
Primary Outcome
A composite outcome of either acute myocardial infarction, cardiac arrest, malignant arrhythmia, cardiac-related mortality
Interventions
- OTHER modified HEART score and/or Emergency Department Assessment of Chest pain Risk Score (EDACS)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13,419 participants |
| Start Date | 2018-07-01 |
| Est. Completion | 2020-06-01 |
What the finished NCT03286179 record still lists
NCT03286179 is an observational study that tracks outcomes without assigning an intervention. Its 13,419 participants enrollment target places it among the larger protocols in the corpus.
The record links to 0 conditions, and to 1 intervention - of which modified HEART score and/or Emergency Department Assessment of Chest pain Risk Score (EDACS) is the first listed.
NCT03286179 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03286179 about?
NCT03286179 is a clinical study titled "Standardizing Emergency Work-ups Around Risk Data". Chest pain is the second leading reason for emergency department (ED) visits in the United States. Resource utilization for this ED subpopulation is particularly high, in part due to a dearth of accepted standardized clinical approaches and general overestimation of risk on the part of both provider...
What is the current status of trial NCT03286179?
This trial is currently completed. The enrollment target is 13,419 participants. The study started on 2018-07-01. Estimated completion is 2020-06-01.
What interventions are being tested in trial NCT03286179?
The interventions under investigation include: modified HEART score and/or Emergency Department Assessment of Chest pain Risk Score (EDACS) (OTHER).
Who is sponsoring clinical trial NCT03286179?
This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT05141396 · 13,400 participants · NA
Telehealth-Enabled, Real-time Audit and Feedback for Clinician AdHerence (TEACH)
- NCT06058767 · 13,764 participants · NA
Preschool Hearing Screening
- NCT05991453 · 13,000 participants · NA
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
- NCT07177352 · 13,000 participants · Phase 3
Screening Study to Determine Individuals With Potential Trial Eligibility for Alzheimer's Disease Studies
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI