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Statewide Implementation of Electronic Health Records - Article


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Personal Medical Records

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Clinical Trial: Statewide Implementation of Electronic Health Records

This study is not yet open for patient recruitment.
Verified by Agency for Healthcare Research and Quality (AHRQ) September 2005

Sponsored by: Agency for Healthcare Research and Quality (AHRQ)
Information provided by: Agency for Healthcare Research and Quality (AHRQ)
ClinicalTrials.gov Identifier: NCT00225576

Purpose

To determine the effects of Electronic Health Record use on medication error rates in primary care office practices.

Hypothesis: Adoption of Electronic Health Records through this program will reduce medication errors

Condition Intervention
Medication Errors
 Procedure: Electronic Health Record Implementation

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Prevention, Non-Randomized, Open Label, Historical Control, Factorial Assignment, Safety Study

Further Study Details: 
Primary Outcomes: 1. Medication errors; 2. Near misses; 3. Adverse drug events
Expected Total Enrollment:  2030

Study start: September 2005;  Expected completion: October 2007
Last follow-up: September 2007;  Data entry closure: September 2007

From the practices committed to implementing EHR in early 2005, we will randomly select 5 adult community-based primary care office practices. We will select 5 similar practices not planning to adopt in that time period.

At each of these office practices we will document rates of medication errors for one week prior to the implementation of an EHR using duplicate prescription pads. Two months after the implementation in the adopting group, allowing some time for familiarization with the tool, we will collect two weeks of data using computer-based information (in the adopting arm) and duplicate prescriptions (in the non-adopting arm).

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • All patients of physicians participating in the study.

Exclusion Criteria:

  • Any patients who are not part of a panel of a participating physician

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00225576

Chelsea Jenter, MPH       cjenter@partners.org

Study chairs or principal investigators

David W. Bates, MD, MPH,  Principal Investigator,  Brigham and Women''''s Hospital, Partners Healthcare System Inc.   

More Information

Study ID Numbers:  HS015397
Last Updated:  September 23, 2005
Record first received:  September 22, 2005
ClinicalTrials.gov Identifier:  NCT00225576
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-27


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November 27, 2009



Page Updated: September 17, 2004
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