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Medication Reconciliation in Oncologic Patients

An Integrated Model to Increase Medication Recognition and Reconciliation in Oncologic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04796142
Acronym
PROF2
Enrollment
100
Registered
2021-03-12
Start date
2019-06-12
Completion date
2023-09-15
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medication Reconciliation

Keywords

Medication reconciliation, IT platform, Pharmacies

Brief summary

To improve medication reconciliation in oncologic patients in healthcare transitions through an alliance between a Cancer Institute and the community pharmacies and a new integrated IT platform.

Detailed description

This trial will explore the alliance between a Cancer Institute and the community pharmacies to improve medication reconciliation in healthcare transitions, and will validate a new integrated IT platform. Cancer patients receiving an oncologic treatment will be asked to choose a pharmacy participating to the trial, and to perform the pharmacological survey before every cycle of chemotherapy. This will be sent through the new IT platform to the electronic medical record of IRST, and the Oncologist will perform the reconciliation. Data about concomitant medications and possible interactions will be exensively analyzed.

Interventions

OTHERmedication reconciliation

medication reconciliation

Sponsors

Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult ≥18 years old * Eastern Cooperative Oncology Group (ECOG) performance status ≤1 * Patients receiving an anticancer treatment * Clear understanding of the Italian language; written informed consent.

Exclusion criteria

\- None

Design outcomes

Primary

MeasureTime frameDescription
medication recognition and reconciliation maintenanceAt day 1 of each cycle of treatment (each cycle might be 14, 21 or 28 days)number of reconciliations per patient

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026