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Comprehensive Medication Monitoring on Heart Failure Patient Outcomes

Primary Purpose

Heart Failure,Congestive

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sano Patient Medication Profile
Sponsored by
Precera Bioscience, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Heart Failure,Congestive focused on measuring clinical decision support, drug levels in blood, therapeutic drug monitoring, medication adherence, medication therapy management

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients must have a regularly scheduled visit to a University of Pittsburgh Medical Center (UPMC) cardiology clinic in Oakland
  • Patients must have Heart Failure with Reduced Ejection Fraction (≤40%)
  • Patients have admitted to UPMC hospital facility between one and five times in past 12 months
  • Patients must be able to provide informed consent for present study
  • Patient age > 18 years

Exclusion Criteria:

  • Enrolled in Hospice
  • Patient on home inotrope (Dobutamine or milrinone)
  • World Health Organization (WHO) Group 1 or Group 5 pulmonary hypertension
  • Patient with current ventricular assist device (VAD)
  • Not able to communicate in English

Sites / Locations

  • UPMC Heart and Vascular Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Heart failure care with Sano test

Heart failure care as-usual

Arm Description

Scheduled outpatient care for patients at high risk of admission for heart failure, supplemented with the Sano Patient Medication Profile

Scheduled outpatient care for patients at high risk of admission for heart failure, care as-usual (i.e. without the Sano Patient Medication Profile).

Outcomes

Primary Outcome Measures

Change in adherence to prescribed cardiology medications
For each patient, the proportion of prescribed medications that are detected using the baseline and final PMP will be calculated; change in adherence will be defined as proportion using final PMP, minus proportion using baseline PMP. Compare adherence difference in intervention vs. control groups.

Secondary Outcome Measures

Number of hospital admissions per patient within 90 days of enrollment in intervention vs. control group
Baseline adherence to prescribed cardiology medications as a predictor of hospital admission for heart failure within 90 days
Baseline adherence to prescribed cardiology medications as a predictor of hospital admission for heart failure within 90 days. This endpoint will use baseline adherence and the Patient Medication Profile will not have been discussed with the care team in the intervention group, therefore both intervention and control groups will be pooled
Drug Related Problem identification and resolution
Documented drug related problems identified by medication reconciliation will be compared between the intervention and control groups. The number of changes in medications to resolve drug related problems, such as medication additions, terminations, dosage or frequency changes will be compared between the intervention and control groups.

Full Information

First Posted
April 26, 2018
Last Updated
January 23, 2019
Sponsor
Precera Bioscience, Inc.
Collaborators
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT03519477
Brief Title
Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
Official Title
A Pilot Prospective, Randomized Controlled Trial Assessing the Impact of Clinical Decision Support Using Comprehensive Medication Monitoring on Heart Failure Patient Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Study terminated by sponsor for commercial reasons
Study Start Date
September 2018 (Anticipated)
Primary Completion Date
January 21, 2019 (Actual)
Study Completion Date
January 21, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Precera Bioscience, Inc.
Collaborators
University of Pittsburgh

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the clinical utility of comprehensive medication monitoring using the Patient Medication Profile to improve heart failure patient medication therapy and associated outcomes relative to usual care in a hospital setting.
Detailed Description
Congestive heart failure has an exceptionally high rate of hospital admission and is responsible for more re-admissions (23.5% at 30 days) in the United States than the 2nd and 3rd leading causes combined. Inadequate medication reconciliation both on admission and discharge from the hospital is a significant cause of medical error. In one study of cardiovascular patients, 44% believed they were taking a medication they were not, and 96% were unable to recall at least one medication they were taking. In the same study patients omitted on average 6.8 medications from their medication list. Medication optimization through improved adherence and reconciled medical records has been postulated to significantly improve admission and 30-day hospital readmission rates. Sano has developed a blood-based comprehensive medication monitoring tool that identifies and quantitates 235 prescription drugs and drug metabolites. It does not detect illicit drugs. This tool, which produces an output report designated the 'Patient Medication Profile', is designed to be used with clinical decision support to improve medication adherence, reduce medication errors, and optimize medication therapy. For heart failure patients, the investigators hypothesize that deploying the Patient Medication Profile with clinical decision support at key points of treatment intervention will A) improve medication adherence, B) identify and reconcile significant discrepancies in the medication list, C) result in reduced hospital admissions, and D) result in better overall patient outcomes. These outcome expectations are relative to usual care for heart failure patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure,Congestive
Keywords
clinical decision support, drug levels in blood, therapeutic drug monitoring, medication adherence, medication therapy management

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Heart failure care with Sano test
Arm Type
Experimental
Arm Description
Scheduled outpatient care for patients at high risk of admission for heart failure, supplemented with the Sano Patient Medication Profile
Arm Title
Heart failure care as-usual
Arm Type
No Intervention
Arm Description
Scheduled outpatient care for patients at high risk of admission for heart failure, care as-usual (i.e. without the Sano Patient Medication Profile).
Intervention Type
Diagnostic Test
Intervention Name(s)
Sano Patient Medication Profile
Intervention Description
The Sano Patient Medication Profile (PMP) is a graphical report comparing prescribed medications to liquid (chromatography/tandem mass-spectrometry) LC/MS/MS-detected drugs from patient blood samples
Primary Outcome Measure Information:
Title
Change in adherence to prescribed cardiology medications
Description
For each patient, the proportion of prescribed medications that are detected using the baseline and final PMP will be calculated; change in adherence will be defined as proportion using final PMP, minus proportion using baseline PMP. Compare adherence difference in intervention vs. control groups.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Number of hospital admissions per patient within 90 days of enrollment in intervention vs. control group
Time Frame
90 days
Title
Baseline adherence to prescribed cardiology medications as a predictor of hospital admission for heart failure within 90 days
Description
Baseline adherence to prescribed cardiology medications as a predictor of hospital admission for heart failure within 90 days. This endpoint will use baseline adherence and the Patient Medication Profile will not have been discussed with the care team in the intervention group, therefore both intervention and control groups will be pooled
Time Frame
90 days
Title
Drug Related Problem identification and resolution
Description
Documented drug related problems identified by medication reconciliation will be compared between the intervention and control groups. The number of changes in medications to resolve drug related problems, such as medication additions, terminations, dosage or frequency changes will be compared between the intervention and control groups.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have a regularly scheduled visit to a University of Pittsburgh Medical Center (UPMC) cardiology clinic in Oakland Patients must have Heart Failure with Reduced Ejection Fraction (≤40%) Patients have admitted to UPMC hospital facility between one and five times in past 12 months Patients must be able to provide informed consent for present study Patient age > 18 years Exclusion Criteria: Enrolled in Hospice Patient on home inotrope (Dobutamine or milrinone) World Health Organization (WHO) Group 1 or Group 5 pulmonary hypertension Patient with current ventricular assist device (VAD) Not able to communicate in English
Facility Information:
Facility Name
UPMC Heart and Vascular Institute
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
20013875
Citation
Cumbler E, Wald H, Kutner J. Lack of patient knowledge regarding hospital medications. J Hosp Med. 2010 Feb;5(2):83-6. doi: 10.1002/jhm.566.
Results Reference
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PubMed Identifier
28461599
Citation
Gupta P, Patel P, Strauch B, Lai FY, Akbarov A, Maresova V, White CMJ, Petrak O, Gulsin GS, Patel V, Rosa J, Cole R, Zelinka T, Holaj R, Kinnell A, Smith PR, Thompson JR, Squire I, Widimsky J Jr, Samani NJ, Williams B, Tomaszewski M. Risk Factors for Nonadherence to Antihypertensive Treatment. Hypertension. 2017 Jun;69(6):1113-1120. doi: 10.1161/HYPERTENSIONAHA.116.08729. Epub 2017 May 1.
Results Reference
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Comprehensive Medication Monitoring on Heart Failure Patient Outcomes

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