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RECRUITING
NCT03470467

Posterior Reversible Encephalopathy Syndrome in the Critically Ill Patients

Sponsor: Ictal Group

View on ClinicalTrials.gov

Summary

Posterior Reversible Encephalopathy Syndrome prospective (PRES) registry. Data collection using a standardized form : demographic data and data related to the PRES, including circumstances of onset, dates and times of onset and of symptoms control, on-scene clinical findings, clinical and radiological features of PRES, pre-hospital and hospital care providers, timing of antiepileptic, antihypertensive drugs and supportive treatments, results of etiological investigations, cause of PRES, type and dosage of antiepileptic and antihypertensive drugs. Dates and times of EEG monitoring, EEG results, radiological and biological investigations. Outcomes including vital status and Glasgow Outcome Scale score at ICU and hospital discharge, day-90 and 1-year after SE and determined based on data in the ICU and/or neurologist charts and/or patients phone interview

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

300

Start Date

2018-03-09

Completion Date

2028-12-31

Last Updated

2019-08-08

Healthy Volunteers

Yes

Interventions

OTHER

No intervention

No intervention planed

Locations (1)

Intensive Care Unit - Versailles Hospital

Le Chesnay, France