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HDL Dysfunction During the Acute Stage of Stroke

HDL Dysfunction During the Acute Stage of Stroke

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03245957
Acronym
RUSH
Enrollment
112
Registered
2017-08-10
Start date
2017-10-20
Completion date
2020-03-31
Last updated
2019-03-07

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

Conditions

Stroke, Acute

Brief summary

The study investigates the effect of plasma myeloperoxidase (MPO) concentrations on HDL dysfunction during the acute stage of ischemic and haemorrhagic strokes.

Detailed description

MRI or CT scan are used to confirm the diagnosis of haemorrhagic, ischemic and mimick stroke. Plasma anf HDL-MPO concentrations, as well as potent HDL dysfunction, are compared in the 3 cases. The investigators hypothesis is that MPO concentrations and subsequent HDL dysfunction could be higher in ischemic strokes than in haemorrhagic ones. MPO could be a examined as a potent marker of early stage of ischemic stroke. Plasma MPO levels could also be discriminant regarding the mimick strokes in patient exhibiting stroke clinical picture.

Interventions

OTHERIschemic stroke

Patients with acute stage of stroke clinical picture, with ischemic, haemorrhagic or mimick stroke diagnosed using MRI or CT scan

OTHERHaemorrhagic stroke

Patients with acute stage of stroke clinical picture, with ischemic, haemorrhagic or mimick stroke diagnosed using MRI or CT scan

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Centre Hospitalier Universitaire de la Réunion
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Patients with less than 12 hours stroke clinical signs: * hemiparesis or hemiplegia * unilateral sensitivity disorder * language impairment * balance disorder * dizziness, bilateral or monocular vision totally or partially lost

Exclusion criteria

* Pregnancy * head trauma since the last 3 months * stroke since the last 3 months * myocardial infarction since the last 3 months * patient disagrees to be enrolled in the study

Design outcomes

Primary

MeasureTime frameDescription
Plasma MPO concentrationsThrough study completion, an average of 6 hoursAssessment of plasma MPO concentrations during acute stage of stroke

Secondary

MeasureTime frameDescription
HDL-MPO concentrationsThrough study completion, an average of 6 hoursAssessment of HDL-MPO concentrations during acute stage of stroke

Other

MeasureTime frameDescription
HDL dysfunctionThrough study completion, an average of 6 hoursAssessment of HDL function using inhibition test on cell culture

Countries

Reunion

Contacts

Primary ContactChristine JUHEL, PHD
christine.juhel@chu-reunion.fr+262262359949
Backup ContactDavid COURET, MD
david.couret@chu-reunion.fr+262262359000

Outcome results

None listed

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