PRecisiOn Medicine In StrokE: Evolution of Plasma Brain-Derived Tau in Acute Stroke
PROMISE-BD-100
PRecisiOn Medicine In StrokE Study on the Evolution of Plasma Brain-Derived Tau in 100 Patients With Acute Ischemic Stroke
1 other identifier
observational
100
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2023
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2023
CompletedFirst Submitted
Initial submission to the registry
October 23, 2023
CompletedFirst Posted
Study publicly available on registry
November 7, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
September 4, 2025
September 1, 2025
3.3 years
October 23, 2023
September 2, 2025
Conditions
Keywords
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.
Interventions
Plasma levels of BD-tau will be assessed using a single-molecule array assay.
Eligibility Criteria
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
Related Publications (25)
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PMID: 21799045BACKGROUND
Biospecimen
Plasma
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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
- 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.
Anonymized individual participant data, including data dictionaries, that underlie results in a publication, will be made available.