Alleviating Geriatric Inpatients' Medication-related Iatrogenesis
NCT ID: NCT05017948
Last Updated: 2024-11-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2021-09-15
2023-11-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Medication Reviews Performed in High Risk Patients
NCT01819974
Improving Safety After Hospitalization in Older Persons on High-Risk Medications
NCT02781662
The Geriatric Emergency Department Pharmacologic Harm Prevention Project
NCT07216846
Reducing Transition Drug Risk
NCT00370916
Medication Reconciliation in Comparison to an Extensive Medication Safety Check
NCT02413957
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
Discharge medication regimen instructions will be provided upon discharge after being assessed using the MWRS, optimized, and assessed by the prescriber.
Risk score based intervention
Targeted interventions based off of risk score software
Standard of Care
Discharge medication regimen instructions will be provided upon discharge after being assessed by the prescriber.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Risk score based intervention
Targeted interventions based off of risk score software
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Prescribed at least 5 medications at hospital discharge
* Baseline medication risk score of 20 or more
Exclusion Criteria
* Discharge to hospice
* Discharge against medical advice
* Patient expiration during initial hospitalization
18 Years
90 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Rutgers, The State University of New Jersey
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Luigi Brunetti
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Robert Wood Johnson University Hospital Somerset
Somerville, New Jersey, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Pro2021001087
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.