Risk Factors for Potential Drug -Drug Interactions: Study in Surgical Intensive Care Unit -Zagazig University Hospitals.

September 1, 2019 updated by: Liza Elsayed Ali soliman shallouf, Zagazig University

Risk Factors for Potential Drug -Drug Interactions: Study in Surgical Intensive Care Unit -Zagazig University Hospitals

Drug drug interactions is frequent in critically ill patients due to polypharmacy, different drug groups and prolonged ICU or hospital stay

Study Overview

Detailed Description

This cross sectional study was conducted in Surgical ICU, zagazig University Hospital for 6months period.

Demographic data (age, gender),clinical history data (main diagnosis, ICU stay in days, transfer from emergency room or other departments, on mechanical ventilation or not, state of consciousness

Study Type

Observational

Enrollment (Actual)

120

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

    • Sharquia
      • Zagazig, Sharquia, Egypt, 33735
        • Liza Elsayed Ali

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

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All patients admitted to Surgical ICUs, zagazig University Hospital

Description

Inclusion Criteria:

  • all patients admitted to Surgical ICUs for six months period

Exclusion Criteria:

  • less than one day admission to ICU,not completed data

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

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Severity of Drug interactions by Lexicomp interactions application
Time Frame: 6months period

Lexicomp interactions classified As:

A(no known interactions) B(no action needed) C(monitor therapy) D(consider therapy modification) X (avoid combination)

6months period
Severity of Drug interactions by Medescape interactions checker:
Time Frame: 6months period
Interactions classified with Medescape interactions checker as :(contraindicated, serious use alternative, monitor closely,minor)
6months period

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Liza Shallouf, Zagazig University
  • Study Director: Heba Matar, Zagazig University

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)

June 15, 2018

Primary Completion (Actual)

January 15, 2019

Study Completion (Actual)

April 20, 2019

Study Registration Dates

First Submitted

August 25, 2019

First Submitted That Met QC Criteria

September 1, 2019

First Posted (Actual)

September 6, 2019

Study Record Updates

Last Update Posted (Actual)

September 6, 2019

Last Update Submitted That Met QC Criteria

September 1, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 4606/28-5-2018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

All data could be shared

IPD Sharing Time Frame

For indefinite time

IPD Sharing Access Criteria

Easy, direct information are available for other researchers

IPD Sharing Supporting Information Type

  • Study Protocol

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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