LMU University hospital, Munich
Munich, Bavaria, 81377, Germany
NCT Number: NCT04315922
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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Notify Me50 year and older
All sexes
Observational
Munich, Bavaria, 81377, Germany
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For the severe stroke cohort, eligibility is defined by:
For the mild stroke cohort, eligibility is defined by:
For the TIA cohort, eligibility is defined by:
Exclusion criteria
Flow Cytometry, Mass-Spectometry, Shotgun-Sequencing
Time frame: 1-7 Days and 90 Days after Stroke
Gut Microbiome Composition is assessed using Shotgun Sequencing
Time frame: 1-7 Days and 90 Days after Stroke
The Metabolome is measured using Mass-Spectometry
Time frame: 1-7 Days and 90 Days after Stroke
Immune Populations are measured using Flow Cytometry
Time frame: 1-7 days and 90 days after stroke
Time frame: 1-7 days and 90 days after stroke
Time frame: 1-7 days and 90 days after stroke
Ludwig-Maximilians - University of Munich
Other
Acronym: SMB
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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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