Hold Parameters on Likely Cardiovascular Depressant Medications
Withdrawn before enrolling
Conditions studied: Asystole, Bradycardia, Hypotension
In brief
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?
Key facts
- Study ID
- NCT00527709
- Run by
- Hackensack Meridian Health
- People needed
- 0
- Starts
- 2006-08-01
- Expected to finish
- 2006-08-01
- Last updated by the study team
- 2020-08-05
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
Where it is running
- Hackensack University Medical Center — Hackensack, New Jersey, United States
Full record on ClinicalTrials.gov
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