Improving Metoclopramide Prescribing Practices at Penn Through a Physician-targeted Intervention

NACompletedINTERVENTIONAL
Enrollment

85

Participants

Timeline

Start Date

March 31, 2007

Primary Completion Date

April 30, 2008

Study Completion Date

April 30, 2008

Conditions
Gastroesophageal Reflux DiseaseDiabetic Gastroparesis
Interventions
OTHER

intervention letter

"Physicians in the intervention group were mailed a written feedback letter regarding their patients who were prescribed questionable metoclopramide therapy. Non-intervention providers received no letter. The letter consisted of the following components:~1. The name and medical record # of the patients involved~2. Information regarding the metoclopramide prescription: dates, dosage, indication recorded, and the duration of therapy~3. A reminder of the adverse effect of long-term metoclopramide therapy~4. A recommendation to consider having the patient undergo a trial of metoclopramide discontinuation if appropriate, and documentation of a discussion of risk and benefits of metoclopramide therapy with patients~5. A request that the physician document the discontinuation trial in the electronic medical record"

Trial Locations (1)

19104

University of Pennsylvania Center for Clinical Epidemiology and Biostatistics, Philadelphia

All Listed Sponsors
lead

University of Pennsylvania

OTHER

NCT01126034 - Improving Metoclopramide Prescribing Practices at Penn Through a Physician-targeted Intervention | Biotech Hunter | Biotech Hunter