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Electronic Health Record (EHR)-Based Intervention for Gastroesophageal Reflux Disease (GERD) and Chronic Non-steroidal Anti-inflammatory Drug (NSAID) Use

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

GERD

Study type

Observational

Funder types

Industry

Identifiers

NCT00691171
NIS-GUS-DUM-2007/1

Details and patient eligibility

About

The purpose of the study is to examine the impact of augmented, high-quality physician-coordinated care executed via an electronic health record (EHR)-based intervention on quality of care for gastroesophageal reflux disease (GERD) and for gastroprotection for patients on chronic non-steroidal anti-inflammatory drugs (NSAIDs) at increased risk for upper GI tract ulcers and ulcer related complications.

Enrollment

5,234 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Eligibility as determined by criteria for participation in studies as part of the MQIC
  • Agreement of participating clinical practices to undergo training in the electronic health record (EHR) intervention designed for this study

Exclusion criteria

  • Based on voluntary participation by MQIC practices, so practices were excluded if they decided to opt out

Trial design

5,234 participants in 3 patient groups

1
Description:
GERD: Patients with established diagnoses of GERD based on ICD-9 codes
2
Description:
Atypical GERD: Patients without an established diagnosis of GERD with atypical symptoms that could be due to GERD (e.g., asthma)
3
Description:
Chronic NSAID users: Patients using chronic NSAIDs who are at increased risk of GI complications (defined as previous diagnosis of peptic ulcer disease; age 75 or older; or concomitant use of corticosteroids, anticoagulants, or aspirin)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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