Study on the development and feasibility of a side effect monitoring program: a preliminary single-arm study

Not Applicable

• Conditions: Diabetes

• Registration Number: JPRN-UMIN000043919
• Lead Sponsor: Osaka Medical and Pharmaceutical University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-05-01
• Study Completion: 2022-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients receiving home visiting drug management guidance by pharmacists 2) Patients who are unable to answer the questionnaire by themselves 3) First-time visitors

Study & Design

• Study Type: Interventional
• Study Design: Not specified