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N/A N=2,596 Randomized Double-blind Treatment

Pragmatic Trial of Messaging to Providers About Treatment of Hyperlipidemia (PROMPT-LIPID)

High Risk Atherosclerotic Cardiovascular Disease

Enrolled (actual)
2,596
Serious AEs
0.0%
Results posted
Sep 2024
Primary outcome: Primary: Proportion of Patients With Intensification of Lipid Lowering Therapy — 159; 142 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Electronic Alert (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Yale University
Primary completion
Jun 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Proportion of Patients With Intensification of Lipid Lowering Therapy
159; 142
SECONDARY
Achieved LDL-C at 6 Months
83; 83
SECONDARY
Proportion of Patients With an LDL-C of Less Than 70 mg/dL
115; 133
SECONDARY
Proportion of Patients With an LDL-C of Less Than 55 mg/dL
45; 53

Summary

This study is designed to evaluate the efficacy of automated electronic alerts in the electronic health record to improve rates of best practices in the treatment of patients with hyperlipidemia who present in the setting of outpatient primary care and family medicine practices within the Yale New Haven Health System.

Eligibility Criteria

Inclusion Criteria for Patient Subjects:

  • Adults 18 years of age or greater
  • Currently being seen as an outpatient of Internal Medicine or Cardiology within the Yale New Haven Health System
  • At very high risk for ASCVD, defined by a history of a major ASCVD event, and most recent lipid profile with LDL-C greater than 70 mg/dL, with or without other high-risk features (diabetes, CKD, age >65 years)

Exclusion Criteria for Patient Subjects:

  • Heart transplant recipient
  • Left ventricular assist device recipient
  • Hospital inpatient status
  • Pregnancy
  • Have opted out of clinical research in MyChart

Inclusion Criteria for Provider Subjects:

  • Practicing at an outpatient cardiology or internal medicine practice with the Yale New Haven Health System
  • High frequency of eligible patients seen, based on retrospective review of outpatient records
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04394715). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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