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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02008604
Other study ID # GUTSTROKE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2014
Est. completion date April 2018

Study information

Verified date November 2018
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to verify the hypothesis that the microbial colonisation of the gut is changed in patients after stroke and that the gut microbiome of severely affected stroke patients differs from that of patients with only a short disruption of blood circulation in the brain (transient ischemic attack, TIA). For this, the composition of gut microbiota in stool samples will be analyzed by 454 pyrosequencing. Further, the correlation of stroke-associated changes in the microbiome with immunological parameters will be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date April 2018
Est. primary completion date April 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age: 18 and older

- ischemic cerebral infarction within the last 40 hours, anterior circulation infarct (ACA, MCA) and/or posterior circulation infarct (PCA, BA) of any severity

- patient consent or consent by a legal representative

- NIHSS > or =9 (stroke patients)

- NIHSS < 1 (for TIA patients)

Exclusion Criteria:

- intracranial hemorrhage

- preexisting dysphagia

- signs of infection upon admission (clinical/paraclinical)

- existing antibiotic therapy upon admission or within the last 2 weeks before admission

- mechanical ventilation upon admission

- participation in an interventional therapy study

Study Design


Locations

Country Name City State
Germany Charite Universitätsmedizin Berlin Berlin

Sponsors (5)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Dr. Christian Meisel, Medical Immunology, Charité Berlin, Germany, NeuroCure Clinical Research Center, Charite, Berlin, PD Dr. Andreas Nitsche, Robert-Koch-Institut, Berlin, Germany, Prof. Dr. Ulrich Dirnagl, Experimental Neurology, Charité Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary composition of intestinal microbiome The composition of the intestinal metagenome / microbiome will be determined by analyzing the 16S rRNA by 454 Pyrosequencing. change between day 1, day 4, day 7, day 14 after stroke
Secondary test of correlation between most changed group of bacteria with changes in immunological parameters (HLA-DR) Analysis of correlation between changes in microbiome (most changed group of bacteria, e.g. lactobacilli) with changes in immunological parameters (e.g. HLA-DR, IL-6, IL-10, CD4-lymphocytes from blood samples). days 1, 4, 7 after stroke
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