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Clinical Trials/NCT04796142
NCT04796142CompletedNot Applicable

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

Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS2 sites in 1 country100 target enrollmentStarted: June 12, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
2
Primary Endpoint
medication recognition and reconciliation maintenance

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts 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

  • Not provided

Outcomes

Primary Outcomes

medication recognition and reconciliation maintenance

Time Frame: At day 1 of each cycle of treatment (each cycle might be 14, 21 or 28 days)

number of reconciliations per patient

Secondary Outcomes

No secondary outcomes reported

Investigators

Study Sites (2)

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