Study Stopped
Due to recruiting issues
Reducing Cost of Azythromycin by Transferring From IV to Oral Therapy
Can the Cost of Azythromycin in be Reduced in Hospitalized Patients With Community Acquired Pneumonia by Quick Transfer From Intravenous to Oral Therapy?
1 other identifier
interventional
N/A
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Dec 2012
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2012
CompletedFirst Submitted
Initial submission to the registry
December 2, 2012
CompletedFirst Posted
Study publicly available on registry
December 5, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedAugust 31, 2016
August 1, 2016
3 years
December 2, 2012
August 30, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
length of intravenous azythromycin treatment
6 months
Study Arms (1)
Before, After
EXPERIMENTALThe intervention is educational
Interventions
after a baseline period, shorter intravenous treatment will be promoted by mail, posters, lectures, and pharmacy monitoring of treatment
Eligibility Criteria
You may qualify if:
- All patients hospitalized with community acquired pneumonia treated by azythromycin
You may not qualify if:
- Age under 18
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Haemek Medical Center
Afula, Israel
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lee H Goldstein, MD
haemek medical center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lee Goldstein MD
Study Record Dates
First Submitted
December 2, 2012
First Posted
December 5, 2012
Study Start
December 1, 2012
Primary Completion
December 1, 2015
Study Completion
December 1, 2015
Last Updated
August 31, 2016
Record last verified: 2016-08