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CASTRO1 - Study on CRP Apheresis After Ischemic Stroke

Not Applicable
Terminated
Conditions
Stroke, Ischemic
Interventions
Device: CRP apheresis
Registration Number
NCT04417231
Lead Sponsor
Pentracor GmbH
Brief Summary

CASTRO1 is a study to investigate the reduction of C-reactive protein (CRP) by therapeutic apheresis (CRP-apheresis) in patients after primary treatment of ischemic stroke.

The term therapeutic apheresis commonly refers to medical procedures, where pathogenic constituents are being removed from the circulating blood. Elimination is performed by adsorbers outside the body in an extracorporeal circulation. For removal of the pathogenic substances the plasma is separated from the blood (circulation) to pass the adsorber. The purified plasma is merged with the solid blood components thereafter and returned to the patient.

The adsorber "PentraSorb® CRP" used for CRP apheresis is CE-certified. It is designated to the selective depletion of C-reactive protein from human blood.

Detailed Description

The purpose of the study is to evaluate the safety and efficacy of CRP apheresis in patients following ischemic stroke. CRP apheresis is to be conducted with the aim of reducing cerebral damage following the guideline-appropriate primary therapy of ischemic stroke.

A possible protective effect of CRP apheresis will be assessed by clinical scores, laboratory determination of immunologic parameters and determination of the size of the infarct area by magnetic resonance imaging (MRI).

The study will be randomized, controlled and monocentric.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
3
Inclusion Criteria
  • Ischaemic stroke with determination of infarct size by imaging (MRI)
  • NIHSS 1-24
  • CRP increase ≥ 5 mg/l within presumed 72 hours after stroke and/or CRP value > 10 mg/l
  • written informed consent of the patient or his legal representative
Exclusion Criteria
  • age < 18 years
  • Severe dysphagia (danger of aspiration pneumonia)
  • Clinical or laboratory evidence of a severe systemic infection
  • Participation in other interventional studies
  • Contraindications against apheresis therapy
  • Modified Rankin Scale (mRS) before index event ≥ 3
  • Intracranial hemorrhage
  • Epileptic seizure in the context of the acute event
  • Pregnancy, lactation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Apheresis groupCRP apheresis10 patients receive a maximum of 3 apheresis treatments at intervals of 24 ± 12 hours each (from the beginning of the preceding treatment). The first treatment starts within 72 hours after infarction or, in case of an unclear time window, within presumed 72 hours after the patient was last seen free of symptoms. No further treatments are carried out if the CRP concentration before the start of a treatment is \<10 mg/l or if the patient has been discharged from hospital. For each treatment, 1.5 - 2.5 times the plasma volume is processed. The duration of each treatment is approximately 4-6 hours.
Primary Outcome Measures
NameTimeMethod
Safety of CRP apheresis24 hours after each apheresis

Incidence of expected and unexpected adverse effects

Secondary Outcome Measures
NameTimeMethod
Concentration of inflammatory biomarkers (CRP, IL-6, SAA)0-7 days after infarction

CRP, Interleukin-6, and serum amyloid A are determined twice daily until discharge of the patient (for a maximum of 7 days).

Stroke Severitybefore first apheresis and 6 ± 3 days after infarction and 12 ± 2 weeks after infarction

National Institute of Health Stroke Scale (NIHSS) score - ranging from 0-42 - higher values represent a worse outcome

Infarct size6 ± 3 days after infarction and 12 ± 2 weeks after infarction

Infarct growth measured via diffusion-weighted imaging (DWI)-FLAIR volume change

Functional Outcomebefore first apheresis and 6 ± 3 days after infarction and 12 ± 2 weeks after infarction

Modified ranking scale (mRS) score - ranging from 0-6 with higher scores signifying worse outcome

Dependency6 ± 3 days after infarction and 12 ± 2 weeks after infarction

Barthel Index (BI) - ranging from 0-100 with higher scores signifying better outcome

Trial Locations

Locations (1)

Abteilung für Neurologie, Universität Ulm

🇩🇪

Ulm, Bayern, Germany

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