Hypotension Clinical Trial
Official title:
Hold Parameters on Likely Cardiovascular Depressant Medications (HOLD)
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Status | Withdrawn |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 |
Verified date | August 2020 |
Source | Hackensack Meridian Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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?
Status | Withdrawn |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. |
Country | Name | City | State |
---|---|---|---|
United States | Hackensack University Medical Center | Hackensack | New Jersey |
Lead Sponsor | Collaborator |
---|---|
Hackensack Meridian Health |
United States,
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