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Imaging and Serological Biomarkers of Autonomic Dysfunction After Ischemic Stroke

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The goal of this observational study is to * to investigate the prevalence and time course of autonomic dysfunction in acute ischemic stroke patients; * to evaluate the influence of lesion location on autonomic dysfunction; * to identify patterns of structural and functional brain connectivity within the central autonomic control circuits associated with autonomic dysfunction; and * to explore causal models of the link between brain lesions; cardiac, immunological and endocrine biomarkers; and dysautonomia. Researchers will compare patients with acute ischemic stroke to patients with transient ischemic attacks to study the effect of acute ischemic brain lesions. Participants will * undergo cardiovascular autonomic function testing; * receive structural and functional MR imaging; * provide blood samples for determinaton of serological biomarkers auf dysautonomia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of either

‣ acute ischemic stroke with either an ischemic lesion visible on CT/MRI or persistent focal deficits 24 hours after symptom onset, or

⁃ Transient ischemic attack with transient clinical deficits including motor or speech disturbance and not restricted to isolated vertigo/dizziness, visual disturbance, or sensory disturbance.

• symptom onset within 72h prior to hospital admission,

• a pre-stroke/TIA ability to walk without help from another person (modified Rankin scale score \< 4),

• age \> 18 years, and

• informed consent by either the patient or a legal representative (including a spouse)

Locations
Other Locations
Germany
University Medical Center Hamburg-Eppendorf
RECRUITING
Hamburg
Contact Information
Primary
Eckhard Schlemm
e.schlemm@uke.de
+49 152 228 98447
Backup
Thies Ingwersen
thi.ingwersen@uke.de
+49 152 228 34568
Time Frame
Start Date: 2025-08-04
Estimated Completion Date: 2026-12
Participants
Target number of participants: 100
Sponsors
Leads: Universitätsklinikum Hamburg-Eppendorf

This content was sourced from clinicaltrials.gov

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