Role of cerebral blood flow pulsatility in hypertension related brain damage
- Conditions
- high blood pressurehypertension1004225810057166
- Registration Number
- NL-OMON55544
- Lead Sponsor
- Medisch Universitair Ziekenhuis Maastricht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Patients with essential hypertension
(HTN):
- Essential hypertension (defined as an ambulant blood pressure of >= 130 over
80 mmHg)
- Age 30-90 years,
Normotensive subjects
(NT):
- Normotensive (ambulant blood pressure of <130 over 80
mmHg)
- Age 30-90 years
Patients with essential hypertension (HTN):
- Indication of history-taking, physical examination or routine laboratory
tests of secondary
hypertension
- Chronic renal insufficiency (eGFR<30 mL/min)
- Diabetes mellitus
- Ischemic or valvular heart disease or electrocardiographic evidence of atrial
fibrillation
- Carotid endarterectomy (CEA): high-grade stenosis > 50%
- Hemorrhagic stroke
- Body Mass Index > 32 kg/m²
- Inability to provide informed consent
- Any contraindication for MRI: metallic implants, pacemaker, claustrophobia,
pregnancy, tattoos,
permanent make-up.
- Contraindications for the gadolinium-containing contrast agent: allergic
reaction, eGFR<30
mL/min ,
Normotensive subjects (NT):
- Indication of history-taking, physical examination or routine laboratory
tests of secondary
hypertension
- Chronic renal insufficiency (eGFR<30 mL/min)
- Diabetes mellitus
- Ischemic or valvular heart disease or electrocardiographic evidence of atrial
fibrillation
- Carotid endarterectomy (CEA): high-grade stenosis > 50%
- Hemorrhagic stroke
- Body Mass Index > 32 kg/m²
- Inability to provide informed consent
- Any contraindication for MRI: metallic implants, pacemaker, claustrophobia,
pregnancy, tattoos,
permanent make-up.
- Contraindications for the gadolinium-containing contrast agent: allergic
reaction, eGFR<30
mL/min
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- To determine the difference between the intracerebral blood flow pulsatility<br /><br>(in the MCA and LSA) of patients with hypertension and normotensive subjects. </p><br>
- Secondary Outcome Measures
Name Time Method <p>- To determine the association between hypertension, blood pressure load,<br /><br>cerebral pulsatility and cSVD severity in terms of white matter hyperintensity<br /><br>volume, number of enlarged perivascular lesions, deep infarcts, and cerebral<br /><br>microbleeds.<br /><br><br /><br>- To determine the relation between cerebral blood flow pulsatility, blood<br /><br>pressure and BBB permeability.<br /><br><br /><br>- To determine the association between cerebral blood flow pulsatility and<br /><br>brain perfusion.<br /><br><br /><br>- To determine the relation of the condition of the microcirculation in the<br /><br>retina and cerebral small vessel blood flow in patients with hypertension. </p><br>