NCT06121336

Brief Summary

The investigators recently identified Brain-derived tau (BD-tau) as a sensitive blood-based biomarker for brain injury in acute ischemic stroke: in patients with acute ischemic stroke, plasma BD-tau was associated with imaging-based metrics of brain injury upon admission, increased within the first 24 hours in correlation with infarct progression, and at 24 hours was superior to final infarct volume in predicting 90-day functional outcome. While informing on the relation of BD-tau with imaging-based metrics of brain injury, this cross-sectional study was restricted to BD-tau assessments upon admission and at day 2 and could not inform on key characteristics of the evolution of plasma BD-tau, including when exactly it starts to rise, how long it continues to rise, and how it is determined by infarct characteristics as well as comorbidities. Here, the investigators aim to assess plasma BD-tau every hour from admission to 48 hours after onset to evaluate the hypothesis that BD-tau rises immediately after onset and plateaus between three and 48 hours after onset.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
5mo left

Started Mar 2023

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress89%
Mar 2023Sep 2026

Study Start

First participant enrolled

March 1, 2023

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

October 23, 2023

Completed
15 days until next milestone

First Posted

Study publicly available on registry

November 7, 2023

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Last Updated

September 4, 2025

Status Verified

September 1, 2025

Enrollment Period

3.3 years

First QC Date

October 23, 2023

Last Update Submit

September 2, 2025

Conditions

Keywords

StrokeBrain injuryBiomarkerPathophysiology

Outcome Measures

Primary Outcomes (1)

  • The primary outcome are plasma BD-tau levels in acute ischemic stroke.

    The evolution of BD-tau levels will be characterized by: * the time point when plasma BD-tau levels start to rise after onset (defined as the earliest time point \[in relation to onset\] that showed higher BD-tau levels compared with the previous assessment and lower levels compared with the next assessment), * the type of rise (e.g. linear, exponential, or logarithmic), and * until when plasma BD-tau levels continue to rise (defined as the time point \[in relation to onset\] compared to which BD-tau levels do not increase by ≥ 5 % compared to 1h, 2h, and 3h afterwards). 5 % were chosen without prior knowledge and in an attempt to account for assay-dependent variations of BD-tau quantifications (coefficient of variation 8-9 %)18 while keeping a biologically and clinically plausible value (rather than e.g. 10 %).

    Every hour from admission to 48 hours after onset.

Secondary Outcomes (10)

  • ASPECTS on non-contrast CT

    Upon admission

  • Ischemic core volume on CT perfusion

    Upon admission

  • Regional leptomeningeal collateral score on CT angiography

    Upon admission

  • Final infarct volume

    Between 48 hours after symptom onset and discharge (latest 10 days after onset)

  • Infarct progression

    Between admission and discharge (latest 10 days after onset)

  • +5 more secondary outcomes

Other Outcomes (3)

  • Plasma levels of NfL

    Hourly from admission to 48 hours after onset

  • Plasma levels of GFAP

    Hourly from admission to 48 hours after onset

  • Plasma proteome and metabolome composition

    Hourly from admission to 48 hours after onset

Study Arms (1)

Ischemic Stroke

100 patients admitted to a specialized stroke service because of an acute ischemic stroke due to large- or medium-vessel occlusion within 9 hours of stroke onset. BD-tau levels and other suggested markers of brain injury (e.g.. NfL) will be assessed every hour from admission to 48 hours after onset. Routinely collected clinical data including from neuroimaging will be collected throughout hospitalization. Clinical follow-up will be performed at 3 months.

Diagnostic Test: Plasma levels of BD-tau

Interventions

Plasma levels of BD-tau will be assessed using a single-molecule array assay.

Ischemic Stroke

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients will be recruited upon admission to a tertiary care hospital.

You may qualify if:

  • clinical diagnosis of acute ischemic stroke
  • presentation within 9 hours of symptom onset
  • large- or medium-vessel occlusion (i.e. an occlusion of the ICA, MCA \[segments M1-M4\], ACA \[segments A1-A3\], basilar artery, or PCA \[segments P1 to P3\]) confirmed by CT or MRI angiography
  • at least 18 years of age
  • written informed consent

You may not qualify if:

  • CT or MRI showing intracranial hemorrhage upon admission
  • A history of ischemic stroke, subarachnoid hemorrhage, intracerebral hemorrhage, subdural hematoma, epidural hematoma, CNS tumor, meningitis, or encephalitis within the last three months
  • severe renal dysfunction (eGFR \< 30ml/min/1.73m2)
  • dementia
  • pre-stroke disability defined as a premorbid modified Rankin Scale score \> 1

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

LMU University hospital, LMU Munich

Munich, Bavaria, 81377, Germany

RECRUITING

Related Publications (25)

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    PMID: 31165090BACKGROUND
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    PMID: 33817340BACKGROUND
  • Boulouis G, Lauer A, Siddiqui AK, Charidimou A, Regenhardt RW, Viswanathan A, Rost N, Leslie-Mazwi TM, Schwamm LH. Clinical Imaging Factors Associated With Infarct Progression in Patients With Ischemic Stroke During Transfer for Mechanical Thrombectomy. JAMA Neurol. 2017 Nov 1;74(11):1361-1367. doi: 10.1001/jamaneurol.2017.2149.

    PMID: 28973081BACKGROUND
  • Ospel JM, McDonough R, Demchuk AM, Menon BK, Almekhlafi MA, Nogueira RG, McTaggart RA, Poppe AY, Buck BH, Roy D, Haussen DC, Chapot R, Field TS, Jayaraman MV, Tymianski M, Hill MD, Goyal M; ESCAPE-NA1 investigators. Predictors and clinical impact of infarct progression rate in the ESCAPE-NA1 trial. J Neurointerv Surg. 2022 Sep;14(9):886-891. doi: 10.1136/neurintsurg-2021-017994. Epub 2021 Sep 7.

    PMID: 34493575BACKGROUND
  • Olivot JM, Mlynash M, Inoue M, Marks MP, Wheeler HM, Kemp S, Straka M, Zaharchuk G, Bammer R, Lansberg MG, Albers GW; DEFUSE 2 Investigators. Hypoperfusion intensity ratio predicts infarct progression and functional outcome in the DEFUSE 2 Cohort. Stroke. 2014 Apr;45(4):1018-23. doi: 10.1161/STROKEAHA.113.003857. Epub 2014 Mar 4.

    PMID: 24595591BACKGROUND
  • Lyden P, Buchan A, Boltze J, Fisher M; STAIR XI Consortium*. Top Priorities for Cerebroprotective Studies-A Paradigm Shift: Report From STAIR XI. Stroke. 2021 Aug;52(9):3063-3071. doi: 10.1161/STROKEAHA.121.034947. Epub 2021 Jul 22.

    PMID: 34289707BACKGROUND
  • Nie X, Leng X, Miao Z, Fisher M, Liu L. Clinically Ineffective Reperfusion After Endovascular Therapy in Acute Ischemic Stroke. Stroke. 2023 Mar;54(3):873-881. doi: 10.1161/STROKEAHA.122.038466. Epub 2022 Dec 7.

    PMID: 36475464BACKGROUND
  • Tiedt S, Duering M, Barro C, Kaya AG, Boeck J, Bode FJ, Klein M, Dorn F, Gesierich B, Kellert L, Ertl-Wagner B, Goertler MW, Petzold GC, Kuhle J, Wollenweber FA, Peters N, Dichgans M. Serum neurofilament light: A biomarker of neuroaxonal injury after ischemic stroke. Neurology. 2018 Oct 2;91(14):e1338-e1347. doi: 10.1212/WNL.0000000000006282. Epub 2018 Sep 14.

    PMID: 30217937BACKGROUND
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    PMID: 16123539BACKGROUND
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    PMID: 11062293BACKGROUND
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    PMID: 16009772BACKGROUND
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    BACKGROUND
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    PMID: 10905241BACKGROUND
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Biospecimen

Retention: SAMPLES WITHOUT DNA

Plasma

MeSH Terms

Conditions

StrokeIschemic StrokeCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesBrain IschemiaNervous System DiseasesBrain Injuries

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular DiseasesCraniocerebral TraumaTrauma, Nervous SystemWounds and Injuries

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 23, 2023

First Posted

November 7, 2023

Study Start

March 1, 2023

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

September 4, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

Anonymized individual participant data, including data dictionaries, that underlie results in a publication, will be made available.

Shared Documents
STUDY PROTOCOL, SAP, ANALYTIC CODE
Time Frame
IPD and additional supporting information will become available starting 6 months after publication.
Access Criteria
IPD and additional supporting information will be shared with academic researchers with a reasonable request to the corresponding author of the respective publication.

Locations