Chuvashia Inappropriate Prescribing Study
CHIP
1 other identifier
observational
300
1 country
1
Brief Summary
This is a cross-sectional study based on an outpatient registry. All medical therapy will be registered in order to assess inappropriate prescribing's, in accordance with the criteria PROMPT and BEERS, also in accordance with the officially approved instructions for the use of this medicinal product.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2023
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 12, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 7, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 7, 2024
CompletedFirst Submitted
Initial submission to the registry
February 20, 2025
CompletedFirst Posted
Study publicly available on registry
February 25, 2025
CompletedJune 10, 2025
June 1, 2025
8 months
February 20, 2025
June 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
frequency of inappropriate drug prescriptions
Рrescribing medications in an inadequate dose, with the wrong frequency, and the wrong duration of treatment, failure to prescribe a potentially effective drug in the presence of clinical indications, self-medication was considered irrational treatment and was assessed as the end point. It also includes prescribing medications that are likely to have a negative effect on the course of concomitant pathology, as well as drug interactions, in accordance with the criteria PROMPT and BEERS.
Assessed at baseline
Eligibility Criteria
This is a cross-sectional study based on an outpatient registry. All medical therapy will be registered in order to assess inappropriate prescribing's, in accordance with the criteria PROMPT and BEERS, also in accordance with the officially approved instructions for the use of this medicinal product.
You may qualify if:
- Age \> 50 years old, multimorbidity, signed Patients' Informed Consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Respublikanski Kardiologicheski Dispanser Minzdrava Chuvashii
Cheboksary, Russia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Sergey Martsevich, M.D., Professor
National Medical Research Centre for Therapy and Preventive Medicine, Moscow, Russia
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Month
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 20, 2025
First Posted
February 25, 2025
Study Start
December 12, 2023
Primary Completion
August 7, 2024
Study Completion
August 7, 2024
Last Updated
June 10, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share