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Reducing Cost of Azythromycin by Transferring From IV to Oral Therapy

Primary Purpose

Pneumonia

Status
Withdrawn
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
education
Sponsored by
HaEmek Medical Center, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pneumonia focused on measuring azythromycin, community acquired pneumonia, intravenous, oral

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients hospitalized with community acquired pneumonia treated by azythromycin

Exclusion Criteria:

  • Age under 18

Sites / Locations

  • Haemek Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Before, After

Arm Description

The intervention is educational

Outcomes

Primary Outcome Measures

length of intravenous azythromycin treatment

Secondary Outcome Measures

Full Information

First Posted
December 2, 2012
Last Updated
August 30, 2016
Sponsor
HaEmek Medical Center, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT01741909
Brief Title
Reducing Cost of Azythromycin by Transferring From IV to Oral Therapy
Official Title
Can the Cost of Azythromycin in be Reduced in Hospitalized Patients With Community Acquired Pneumonia by Quick Transfer From Intravenous to Oral Therapy?
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Withdrawn
Why Stopped
Due to recruiting issues
Study Start Date
December 2012 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
HaEmek Medical Center, Israel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Intravenous Azythromycin therapy is considerably more expensive than oral therapy. The investigators believe that intravenous therapy is prolonged more that necessary and that oral therapy can be used much earlier in the course of the disease. The investigators plan to check if that statement is true and intervene in order to shorten the intravenous therapy.
Detailed Description
The study will be performed in two stages. First a retrospective review of medical files of 50 patients hospitalized in the Haemek Medical Center with severe community acquired pneumonia, treated with azythromycin. The files will be reviewed for the criteria clinical improvement, and for azythromycin therapy, oral or intravenous. The results of this review will help us define the appropriate behavioral intervention in order to cause doctors to transfer from IV to PO therapy at the earliest appropriate time. An intervention such as posters, pharmacy overseeing etc will be introduced. 3 months after the intervention, an additional 50 files of pneumonia patients treated with azythromycin will be reviewed in order to check the efficacy of the intervention. The Review board and the NIH will be updated about the intervention, as soon as the investigators have decided what intervention is appropriate

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumonia
Keywords
azythromycin, community acquired pneumonia, intravenous, oral

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Before, After
Arm Type
Experimental
Arm Description
The intervention is educational
Intervention Type
Behavioral
Intervention Name(s)
education
Intervention Description
after a baseline period, shorter intravenous treatment will be promoted by mail, posters, lectures, and pharmacy monitoring of treatment
Primary Outcome Measure Information:
Title
length of intravenous azythromycin treatment
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients hospitalized with community acquired pneumonia treated by azythromycin Exclusion Criteria: Age under 18
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee H Goldstein, MD
Organizational Affiliation
haemek medical center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haemek Medical Center
City
Afula
Country
Israel

12. IPD Sharing Statement

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Reducing Cost of Azythromycin by Transferring From IV to Oral Therapy

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