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Predictive Value of Copeptin in the Diagnosis of Acute Ischemic Stroke

Predictive Value of Copeptin in the Diagnosis of Acute Ischemic Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01960478
Enrollment
150
Registered
2013-10-10
Start date
2014-01-07
Completion date
2014-10-05
Last updated
2021-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Vascular Accident (CVA)

Brief summary

In the USA, every year 795,000 patients suffer a cerebral vascular accident (CVA), which represents a yearly cost of $73.7 billion. CVA is the third main cause of death and the main source of acquired handicap in adults, as a result it is now a key priority in public health and part of The CVA National Action Plan 2013-2014. Copeptin is a polypeptide, by- product of Vasopressin metabolism. The increase of Copeptin plasma level, as for Vasopressin, is connected to hydric balance disorders found in cardio-vascular, renal and endocrine diseases. This link has already shown its interest in the early diagnosis of myocardial infarction and, in a more indirect way, CVA. Copeptin is associated with acute endogenous stress. It seems to have interesting potential in the diagnosis of CVA by its negative predictive value like D-dimeres in pulmonary embolism. Proadrenomedullin and Brain Natriuretic Peptide (BNP) are both associated with the prognosis of cardio-vascular diseases and could be interesting in evaluating CVA prognosis.

Interventions

BIOLOGICAL(for each intervention)
OTHERBlood test

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients, male or female, may be included if they meet the following criteria: * patients with suspected ischemic CVA admitted in an acute stroke unit (thrombolysis unit). * aged 18 and over. * MRI Scan undertaken under the current protocol which includes the following sequences: distribution, T2\* (gradient echo), ARM, TOF and FLAIR. * after information given the consent form is signed: * by the patient .or for those unable to express their consent (in case of coma or severe neurological disorder) by a relative or next of kin. .the patient will be informed as soon as he has recovered his faculties in order to be able to express, if he wishes, his opposition to the pursuit of the research (sample destruction before tested). \- the patient must be registered with the Social Security

Exclusion criteria

All patients with a contraindication to MRI Scan: * Pacemaker, * Implanted cardiac defibrillator, * Implanted Neuro-stimulator, * Cochlear Implants * Implanted Insulin pump * Other implanted electronic medical device * Vascular intracerebral Clip * Cardiac Valve * Other metallic implant * Metallic foreign body * Ventricular diversion valve * Eye or hearing prosthesis * Current or suspected pregnancy * Breast feeding Those who are under protection of justice, under guardianship or curatorship will also be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Determine the minimum level of Copeptin required to determine if the patients present with acute CVA or not.Participants will be followed during 90 daysCopeptin is associated with acute endogenous stress. It seems to have interesting potential in the diagnosis of CVA by its negative predictive value like D-dimers in pulmonary embolism. Proadrenomedullin and Brain Natriuretic Peptide (BNP) are both associated with the prognosis of cardio-vascular diseases and could be interesting in evaluating CVA prognosis

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026