Cerebral Microembolism During Hemodialysis
Last updated on April 2022Recruitment
- Recruitment Status
- Completed
- Estimated Enrollment
- 20
Inclusion Criteria
- Renal replacement therapy (continuous veno-venous hemodilalysis) on the in-house intensive care unit
- Age > 18yrs and < 90yrs
- Renal replacement therapy (continuous veno-venous hemodilalysis) on the in-house intensive care unit
- Age > 18yrs and < 90yrs
Exclusion Criteria
- Allergy against materials of the medical device used in the study (transcranial Doppler) or temporal skin/bone lesions
- Carotid artery stenosis > 70%
- Treatment with other extracorporeal devices
- ...
- Allergy against materials of the medical device used in the study (transcranial Doppler) or temporal skin/bone lesions
- Carotid artery stenosis > 70%
- Treatment with other extracorporeal devices
- Neurocognitive disturbances
- Absent informed consent
- Cardial pathology (valvular heart disease, prosthesis, endocarditis)
- Inclusion in an other clinical study
- Pregnancy, drug abuse
- Patent foramen ovale
- Preexistent neurological morbidity
Summary
- Conditions
- Cerebral Embolism
- Complication of Dialysis
- Thrombus Due to Renal Dialysis Device, Implant, or Graft
- Type
- Observational
- Design
- Observational Model: Case-Only
- Time Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 90 years
- Gender
- Both males and females
Inclusion Criteria
- Renal replacement therapy (continuous veno-venous hemodilalysis) on the in-house intensive care unit
- Age > 18yrs and < 90yrs
- Renal replacement therapy (continuous veno-venous hemodilalysis) on the in-house intensive care unit
- Age > 18yrs and < 90yrs
Exclusion Criteria
- Allergy against materials of the medical device used in the study (transcranial Doppler) or temporal skin/bone lesions
- Carotid artery stenosis > 70%
- Treatment with other extracorporeal devices
- ...
- Allergy against materials of the medical device used in the study (transcranial Doppler) or temporal skin/bone lesions
- Carotid artery stenosis > 70%
- Treatment with other extracorporeal devices
- Neurocognitive disturbances
- Absent informed consent
- Cardial pathology (valvular heart disease, prosthesis, endocarditis)
- Inclusion in an other clinical study
- Pregnancy, drug abuse
- Patent foramen ovale
- Preexistent neurological morbidity
Tracking Information
- NCT #
- NCT02021045
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Gabor Erdoes, MD Medical University of Vienna
- Gabor Erdoes, MD Medical University of Vienna
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