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Completed

NCT Number: NCT04315922

Multiomics Targeting Microbiome Associated Changes in Stroke Patients (StrokeMicroBiomics)

Preclinical research has established a convincing connection between changes in the gut microbiota composition and stroke outcome. However clinical data on the gut-brain axis, and its chronic characteristics, is sparse. Additional investigations in the context of ischemic stroke regarding the relationship between dysbiosis and functional changes of the microbiome, as characterized by the metabolome, are still required. The StrokeMicroBiomics study will offer insight into these mechanisms and offer new potential targets for therapeutic interventions.

The primary objective is the characterisation of gut dysbiosis in ischemic stroke patients in the acute phase after stroke and during a 3 month follow-up period.

The secondary objectives include the identification of dysregulated gut microbiome metabolites and key immune cell populations in addition to the clinical progression of the study participants during the 3 month follow-up period after disease onset.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

LMU University hospital, Munich

Munich, Bavaria, 81377, Germany

About this study

Results of experimental, preclinical studies suggest that microbiome-targeted may improve stroke outcome as well as stroke-related comorbidities. Yet, clinical trials describing the extent and time course of microbiome changes after stroke are currently not available. Moreover, the impact of post-stroke dysbiosis on metabolic changes and the systemic immunity are unexplored.

Therefore, the primary objective of this trial is the characterization of gut dysbiosis progression in ischemic stroke patients during a 3 month follow-up period .

The secondary objectives include the identification of dysregulated gut microbiome metabolites and key immune cell populations in addition to the clinical progression of the study participants during the 3 month follow-up period after disease onset.

In order to elucidate the differential impact of lesion size on immune and microbiome homeostasis, separate patient cohorts with mild and severe stroke will be studied.

Furthermore, to control for the effects of temporary focal neurological deficits and stress induced microbiome and immune changes, patients with stroke mimics and transient ischemic attacks (TIA) are being recruited to the control group.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written consent as submitted and approved to the human subjects review board must be gathered from the participants
  • Participants must be at least 50 years of age

For the severe stroke cohort, eligibility is defined by:

  • CT or MRI confirmed ischemic stroke affecting at least 1/3 of the anterior, medial or posterior cerebral arteries cortical coverage
  • NIHSS of at least 10 at time of induction into emergency room
  • Ischemic Stroke occured within the last 7 days

For the mild stroke cohort, eligibility is defined by:

  • CT or MRI confirmed ischemic stroke affecting no more than 1/3 of the anterior, medial or posterior cerebral arteries cortical coverage
  • NIHSS between 1 and 10 at time of induction into emergency room
  • Ischemic Stroke occured within the last 7 days

For the TIA cohort, eligibility is defined by:

  • CT or MRI confirmed absence of a lesion
  • NIHSS of 0 no more than 24 hours after induction into emergency room
  • TIA occured within the last 7 days

Exclusion criteria

  • Pregnancy
  • Diagnosed and malignant Tumor ailment
  • Active, non-stroke related immunosuppression (i.e. HIV)
  • Infection, operative procedure or antibiotics treatment within 4 weeks prior to stroke/TIA
  • Relevant autoimmune disease (i.e Morbus Crohn)
  • Chronic infectious diseases (i.e Hepatitis C)
  • Hemorrhagic Stroke or intracranial bleeding
  • Cerebellar lesions
  • Other neurodegenerative diseases (i.e. Parkinson´s Disease or Alzheimers Dementia)

Treatment and study plan

Microbiome and Plasma Characterisation

Diagnostic Test

Flow Cytometry, Mass-Spectometry, Shotgun-Sequencing

Primary outcomes

  1. Changes from Baseline in the Gut Microbiome Composition at 3 Months post Stroke/TIA

    Time frame: 1-7 Days and 90 Days after Stroke

    Gut Microbiome Composition is assessed using Shotgun Sequencing

  2. Changes from Baseline of the Gut Metabolome as measured in Blood and Stool at 3 Months post Stroke/TIA

    Time frame: 1-7 Days and 90 Days after Stroke

    The Metabolome is measured using Mass-Spectometry

  3. Changes from Baseline in key Immune Populations at 3 Months post Stroke/TIA

    Time frame: 1-7 Days and 90 Days after Stroke

    Immune Populations are measured using Flow Cytometry

Secondary outcomes

  1. National Institute of Health Stroke Scale (NIHSS)

    Time frame: 1-7 days and 90 days after stroke

  2. Modified Rankin Score (mRS)

    Time frame: 1-7 days and 90 days after stroke

  3. CT and (if available) MRI documentation

    Time frame: 1-7 days and 90 days after stroke

Sponsors and collaborators

Lead sponsor

Ludwig-Maximilians - University of Munich

Other

Collaborators

  • University of Luxembourg

Registry information

Acronym: SMB

Important dates

Study start
2019
Primary completion
2022
Study completion
2023
First posted
Mar 20, 2020
Registry last updated
Oct 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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