Intensive Care Unit Syndrome Clinical Trial
— PAREAOfficial title:
Prospective Study Evaluating the Hemodynamic Impact of PAracetamol Administration in Patients Hospitalized in the REAnimation Intensive Care Unit
NCT number | NCT06430697 |
Other study ID # | 22-AOI-13 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2024 |
Est. completion date | April 2027 |
Paracetamol is commonly used in case of pain or fever. Few previously clinical studies has highlighted an arterial hypotension linked to intravenous administration of paracetamol. Currently, fewer data are available on the link of intravenous administration of paracetamol and effects on arterial tension. The aim of this study is to describe the frequency of occurrence of significative arterial hypotension within one hour following intravenous or per os administration of paracetamol . Other factors who can be associated to occurence of significative arterial hypotension will be also observe (for example age, weight, pain, vasopressor dosage or sedative...)
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | April 2027 |
Est. primary completion date | December 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: Inclusion: - 18 years of age or older - Patient with arterial catheter - Indication of paracetamol's administration by the patient's attending practitioner. - No opposition to patient or support person participation in the study if the patient is unable to participate ExclusionCriteria: - No Social Security Patient - Pregnant or nursing patient. - Patient with a legal protection measure - Hypersensitivity and/or allergy to paracetamol. - Contraindication to the use of paracetamol. - Patient opposition to health data collection. |
Country | Name | City | State |
---|---|---|---|
France | CHU de NICE ARCHET | Nice |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Nice |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measure frequency of low blood pressure following paracetamol administration | Proportion of patients with clinically significant low blood pressure occurring within one hour of administration of paracetamol IV or per os. Clinically significant low blood pressure is defined as an average blood pressure of less than 60 mmHg and/or a decrease in average blood pressure of more than 15%, and/or need for vascular filling and/or initiation or increase of the dose of noradrenaline | One hour after administration of paracetamol | |
Secondary | Measure of blood pressure following paracetamol administration according to IGS II score | Identify patients' predictors of low blood pressure following paracetamol administration : Patients' will be identified by measuring frequency of patients with low blood pressure following paracetamol administration, according to The IGS II score (Simplified Severity Index II) is a score used to assess the severity of a patient and is one of the scores used in intensive care and SOFA score.
Components: The IGS II includes several variables, such as age, chronic health conditions, vital signs, and laboratory values. These factors are combined to calculate a numerical score. Scoring: The higher the IGS II score, the greater the predicted risk of mortality. The score ranges from 0 to 100, with higher values indicating more severe illness. |
One hour after administration of paracetamol | |
Secondary | identify predictors linked to paracetamol administration route | Measure of blood pressure to identify predictors by measuring frequency of patients with low blood pressure following paracetamol administration, according to administration's route | One hour after administration of paracetamol | |
Secondary | identify predictors linked to paracetamol dosage | Measure of blood pressure to identify predictors by measuring frequency of patients with low blood pressure following paracetamol administration, according to dosage | One hour after administration of paracetamol | |
Secondary | Measure of blood pressure following paracetamol administration according to SOFA score | Identify patients' predictors of low blood pressure following paracetamol administration : Patients' will be identified by measuring frequency of patients with low blood pressure following paracetamol administration, according to the SOFA score.
The sequential organ failure assessment score (SOFA score), previously known as the sepsis-related organ failure assessment score,is used to track a person's status during the stay in an intensive care unit (ICU) to determine the extent of a person's organ function or rate of failure. Each system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure). The worst physiological variables are collected serially every 24 hours of a patient's ICU admission12. The total SOFA score ranges from 0 (best) to 24 (worst) points. It's a valuable tool for predicting clinical outcomes in critically ill patients |
One hour after administration of paracetamol |
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