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Hemodynamic Impact of the Administration of PAracetamol in Patients Hospitalized in the Intensive Resuscitation Medicine Department [PAREA]

C

Centre Hospitalier Universitaire de Nice

Status

Not yet enrolling

Conditions

Intensive Care Unit Syndrome

Treatments

Drug: paracetamol administration

Study type

Interventional

Funder types

Other

Identifiers

NCT06430697
22-AOI-13

Details and patient eligibility

About

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...)

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Treatment with paracetamol
Experimental group
Treatment:
Drug: paracetamol administration

Trial contacts and locations

1

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Central trial contact

Kamila BURDZENIDZE, Study nurse

Data sourced from clinicaltrials.gov

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