Trials / Completed
CompletedNCT01126034
Improving Metoclopramide Prescribing Practices at Penn Through a Physician-targeted Intervention
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 85 (actual)
- Sponsor
- University of Pennsylvania · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
The investigators hypothesized that: 1\) an intervention targeted at the prescribing physician would increase the rate of a metoclopramide discontinuation among patients prescribed the medication for questionable or unclear indications; and 2) the discontinuation would be durable.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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 |
Timeline
- Start date
- 2007-03-01
- Primary completion
- 2008-04-01
- Completion
- 2008-04-01
- First posted
- 2010-05-19
- Last updated
- 2015-12-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01126034. Inclusion in this directory is not an endorsement.