A Study on Behavior of Healthcare Professionals Who Handle Oral Solid Drug

January 11, 2024 updated by: Enrico Tomasi

Multicentric Study on Knowledgement and Behaviors of Health Care Professionals Handling Oral Solid Pharmaceutical Forms/Drugs

A study on behavior of healthcare professionals who handle oral solid drug

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

A study on behavior of healthcare professionals who handle oral solid drug

Study Type

Observational

Enrollment (Actual)

45

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Italy
      • Milan, Italy, 20132
        • Irccs Ospedale San Raffaele

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthcare professionals in charge of drug preparation

Description

Inclusion Criteria:

• Healthcare professionals in charge of drug preparation

Exclusion Criteria:

• There are not exclusion criteria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Observation on behavior of healthcare professional workers during hpreparation of oral solid pharmaceutical drug
Time Frame: 3 months
Observation on behavior of healthcare professional workers during hpreparation of oral solid pharmaceutical drug
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Enrico Tomasi

Investigators

  • Principal Investigator: Maria Fazio, IRCCS

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 15, 2021

Primary Completion (Actual)

December 31, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

January 2, 2024

First Submitted That Met QC Criteria

January 11, 2024

First Posted (Actual)

January 22, 2024

Study Record Updates

Last Update Posted (Actual)

January 22, 2024

Last Update Submitted That Met QC Criteria

January 11, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Recommendation n°19

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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