Enhanced Medication Reconciliation For Serious Mental Illness
Stopped early · Not applicable
Conditions studied: Mental Disorders
In brief
The purpose of this study is to evaluate the clinical utility of a decision support tool, the Patient Medication Profile(TM), developed by Sano Informed Prescribing on medication reconciliation and identification of drug-related problems in patients with serious mental illness.
Key facts
- Study ID
- NCT03169868
- Run by
- Precera Bioscience, Inc.
- People needed
- 26
- Starts
- 2018-02-27
- Expected to finish
- 2019-01-21
- Last updated by the study team
- 2019-01-25
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Current insurer is UPMC Health Plan
- Currently active in CRS clinic
- Prescribed four or more medications as indicated by pre-study Health Plan Medication List
- Able to provide informed consent for present study
You may not qualify if…
- Not competent to give informed consent in the opinion of the investigator
- Having had a previous medication reconciliation by the clinical pharmacist
Where it is running
- Western Psychiatric Institute and Clinic of UPMC — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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