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Functional Prognosis in Patients With Ischemic Stroke According to the Therapeutic Strategy Used (PARADISE)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Completed

Conditions

Ischemic Stroke

Treatments

Biological: prise de sang
Other: quality of life questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT02856074
Béjot 2015-2

Details and patient eligibility

About

The current management of ischemic stroke is based on different strategies that may be combined: intravenous thrombolysis in a stroke ICU, intravenous thrombolysis in a telemedicine procedure, endovascular thrombectomy. Given this now rich therapeutic arsenal, it seems necessary to evaluate practices in local care in the field and the impact of these on the prognosis of ischemic stroke victims. The aim of this observational study is to compare these different care practices without interfering with the choice of strategy.

A blood sample will also be taken at different times to study the value of growth differentiation factors (GDF) 8, 11 and 15, and Brain-derived Neurotrophic Factor as prognostic biomarkers

Enrollment

821 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with symptomatic ischemic stroke defined according to WHO criteria and treated by intravenous thrombolysis at the stroke ICU at Dijon CHU, intravenous thrombolysis by telemedicine with subsequent transfer to the Dijon stroke ICU, and/or endovascular thrombectomy at Dijon CHU)
  • Patients aged over 18 years.
  • Patients who have provided written informed consent to take part in the study.

Exclusion criteria

  • Patients who refuse to take part in the study.
  • Subjects in custody.
  • Patients (or a person of trust) who cannot be contacted by telephone during the follow-up.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

821 participants in 1 patient group

Ischemic stroke patients
Experimental group
Treatment:
Biological: prise de sang
Other: quality of life questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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