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Current Use in Intensive Care Units by Intensivists of Antihypertensive Drugs

Conditions
Antihypertensive Drugs in ICU
Registration Number
NCT04924946
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Multicenter, prospective and observational study of practices and impacts of the use of antihypertensive therapies in intensive medicine and intensive care

Detailed Description

Multicenter, prospective observational cohort study on 200 patients, by doctor's questionnaire on the prescription of antihypertensive drugs in intensive care, follow-up over 72 hours of the prescription.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Adult patient
  • Admitted to an intensive care unit
  • Patient having presented a state of circulatory shock, defined by the need for continuous administration of a vasopressive amine for at least one hour, among: Noradrenaline, Adrenaline
  • In whom the introduction of drug treatment for antihypertensive purposes is decided
Exclusion Criteria
  • Patient admitted to intensive care for a hypertensive emergency (hypertensive surge or malignant arterial hypertension leading to organ dysfunction
  • Patient who has already received at least one anti-hypertensive drug during his stay in intensive care
  • Cerebro-injured patient, proven or suspected cerebral edema, head trauma <1 month, decrease in cerebral perfusion measured
  • Proven or suspected active bleeding
  • Patient refusal of participation

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Make an inventory of prescribing habits and detect any differences in efficacy and tolerance of antihypertensive drugs in intensive care and intensive care settings60 days after inclusion

reasons for prescribers

Secondary Outcome Measures
NameTimeMethod
Search for efficiency differences between the different molecules60 days after inclusion

Improved kidney function

Search for differences in side effects between the different molecules60 days after inclusion

Other side effect

Trial Locations

Locations (7)

Intensive Care Victor Dupouy Hospital

🇫🇷

Argenteuil, France

Intensive Care René Dubos Hospital

🇫🇷

Pontoise, France

Intensive Care Bichat Hospital

🇫🇷

Paris, France

Intensive Care Avicenne Hsopital

🇫🇷

Bobigny, France

Intensive Care Tours Hospital

🇫🇷

Tours, France

Intensive Care Longjumeau Hospital

🇫🇷

Longjumeau, France

Intensive Care Louis Mourier Hospital

🇫🇷

Colombes, France

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