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Electronic medication reconciliation

Phase 3

Medication Reconciliation | Unknown | Other |Healthcare Services Group|Last Updated: Mar 5, 2014

Success Probability

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Market & Valuation

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Trial Design

RandomizedNO_TREATMENT_CONTROLLEDDMC
Total Trials1
Total Enrollment4,818

FDA Designations

No designations recorded

Clinical trial landscape

Electronic medication reconciliation · 1 trial · 1 indication

Phase 3 1
NCT01195051Medication Reconciliation Technology to Improve Quality of Transitional CareMedication Reconciliation
COMPLETED4,818 Analytics
PHASE3COMPLETED
Medication Reconciliation Technology to Improve Quality of Transitional Care
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Study Endpoints

Primary Endpoints

Reconciliation of outpatient medications
Hospital admission, transfer, and discharge; 1 year

Number and fraction of outpatient medications prescribed or addressed as to why prescribing did not occur. Number and fraction of cases with MR by a pharmacist. Number and fraction of cases undergoing any MR. Number and fraction of cases where any outpatient medications were not prescribed or addressed as to why prescribing did not occur.

Secondary Endpoints

Measurement of potential for harm and potential severity of harm
Hospital discharge; 1 year
Measurement and analysis of providers' perspectives
Start and end of trial; 1 year
Measurement and analysis of patients' perspectives
Hospital discharge; 1 year
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Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeHEALTH_SERVICES_RESEARCH

Treatment Arms

ArmTypeDescription
Electronic medication reconciliationEXPERIMENTALProviders have access to a new, computer-based application to facilitate documentation and prescribing of outpatient medications in the inpatient setting.
ControlNO_INTERVENTION -

Interventions

NameTypeDescription
Electronic medication reconciliationOTHERA new, computer-based application will be used to document and prescribe outpatient medications in the inpatient setting.
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Patients admitted to the Medicine Service during a 12-month period * Physicians who provide inpatient or ambulatory care for participating patients. * Pharmacists who provide care for participating patients. Exclusion Criteria: * Patients admitted but not seen in a primary-c...

Countries:United States
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Frequently asked questions about Electronic medication reconciliation

What is Electronic medication reconciliation used for?

Electronic medication reconciliation is used for medication reconciliation, the process of comparing a patient's medication orders to all of the medications the patient has been taking. It is designed to improve the quality of transitional care, which is the coordination and continuity of health care during movement between different health care settings.

Who makes Electronic medication reconciliation?

Electronic medication reconciliation is developed by Healthcare Services Group, a company traded on the NASDAQ under the ticker HCSG. The company is conducting clinical development of this medication reconciliation technology.

What phase is Electronic medication reconciliation in?

Electronic medication reconciliation is in Phase 3 clinical development. It is an investigational technology and is not approved for commercial use. The Phase 3 trial has been completed, and the technology is being evaluated for its effectiveness in improving transitional care.

What clinical trials is Electronic medication reconciliation in?

Electronic medication reconciliation has one completed Phase 3 clinical trial, identified as NCT01195051, titled "Medication Reconciliation Technology to Improve Quality of Transitional Care." The trial enrolled 4,818 participants in the United States, with a minimum age of 18 years, and included both male and female participants.

Is Electronic medication reconciliation a randomized controlled trial?

Yes, the Phase 3 clinical trial of Electronic medication reconciliation, NCT01195051, is a randomized trial. It is not double-blind and uses a no-treatment control group. The trial enrolled 4,818 participants and has been completed.