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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00527709
Other study ID # 06.01.025
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date August 2006
Est. completion date August 2006

Study information

Verified date August 2020
Source Hackensack Meridian Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This pilot study is being pursued to observe whether certain medications are given to patients within a timeframe where their being given could play a part in a critical event in the management of the patient.

There are general rules about when it would be appropriate for these types of medications not to be given. However, it is not current standard practice for the criteria to be put in place without the expressed wishes of the ordering physician or their agent.

Research Question:

Can the administration of cardio-depressant medications be documented as a significant risk factor for hypotensive or bradycardic events?


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2006
Est. primary completion date August 2006
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Serial evaluation of the first 50 documented events of Code Blue or call to Rapid Response Team involving hypotension, bradycardia or asystole in the adult inpatient population events beginning January 1, 2006.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Hackensack University Medical Center Hackensack New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Hackensack Meridian Health

Country where clinical trial is conducted

United States, 

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