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Effectiveness of a Postal Intervention to Improve the Use of PPI

NCT03840018 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 401

Last updated 2019-02-15

No results posted yet for this study

Summary

It was a randomised intervention study, with before-and-after outcome measures and a control group, in patients who had an active long-term prescription for PPIs at high doses for at least 6 months.

Conditions

  • Drug Overdose

Interventions

OTHER

Letter by post to patients

Patients received an informative letter by post, in which their doctor invited them to seek an appointment for a medication review

Sponsors & Collaborators

  • Osakidetza

    lead OTHER

Principal Investigators

  • Elena Valverde · Osakidetza

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-10
Primary Completion
2017-12-10
Completion
2018-04-18

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03840018 on ClinicalTrials.gov