Cerebral Perfusion Associated With Postural Changes: an ASL MR Perfusion Study (PerfIRMAVC)

University Hospital Center of Martinique

Status: Completed

Conditions: Brain Ischemia

Treatments: Procedure: MRI

Study type: Interventional

Funder types: Other

Identifiers

NCT02912546

16/B/03

Details and patient eligibility

About

Postural changes are commonly used as therapeutic maneuver to enhance or reduce cerebral perfusion. For instance, in acute stroke, the patient can be positioned in head down tilt position so as to increase perfusion of cerebral tissues perfusion. In During stroke and in hypertensive patients and during stroke, varying degrees a various loss of cerebral autoregulation is loss are usually observed. The aim of this study is to assess cerebral perfusion with ASL perfusion in human subjects in different conditions: healthy, hypertensive and stroke.

Full description

Material and methods:

Eighteen stroke patients, eighteen hypertensive patients and eighteen healthy subjects (men and women) will be enrolled. The investigator will use a 1.5 Tesla MRI device with a large magnet bore (70 cm) allowing positions change. Two measures will be performed, one in supine position and the other in head down position (-20°). A 3D FSE ASL sequence will be acquired and Cerebral Blood Flow (CBF) maps will be reconstructed. Volume of interest (VOI) will be placed on cortical grey matter (frontal and posterior gyrus), on subcortical deep grey matter (caudate nuclei, thalami) and subcortical white matter (semi oval centers). Differences in CBF values (in mL/100g/min) will be analyzed using SAS 9.3 software for Windows (SAS Institute, Cary North Carolina, USA).

Expected results and hypothesis:

CBF is expected to significantly vary between the supine and head down positions. It is expected to at least increase in the head down position, for stroke patients. For healthy subjects and hypertensive patients, cerebral autoregulation may limit CBF increase although an increasing trend for CBF is expected.

Enrollment: 34 patients

Sex: All

Ages: 30 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Group of stroke patients:

   • Patients between 40 and 70 years old, male or female
   • With supratentorial ischemia in subacute phase (> H24)
   • Patients with a recent ischemic stroke with an intracranial hemodynamic unstable and kept lying with head down of about 30
   • Patient given free and informed consent to participate in research or a family representative
   • Patient insured under the French social security system

2. Control Group:

1- Group of patients with Hypertension.

• Patients between 40 and 70 years old, matched for age and sex to stroke patients.

• With a hypertension diagnosed since 10 years old.

• Hypertension defined as three recommendations (OMS 1999, ANAES 1997 JNC VI): blood pressure 140 and / or 90 mmHg found at several consultations.

  2- Group with healthy people.

• Healthy person between 30 and 70 years old, women and men. Healthy character will be defined on the basis of a physical examination (measurement of heart rate and blood pressure ) and an examination to determine the absence of endocrine pathology ... ) and the absence of drug outlet continuous.

• Person insured under the French social security system.

• Person who given free and informed his consent to participate in research or a family representative.

• Person who are not participating in another clinical study.

Exclusion criteria

• Patients aged under 40 years and 71 years and older for patients in groups of stroke patients and patients with hypertension
• Person under 30 years and 71 years and older for healthy people
• Person who refuses or family the participation in the study
• Person with heart antecedent or spinal disease
• Contraindications to the realization of a MRI (pacemaker, claustrophobia, metallic body may be mobilized).
• Person not insured under the French social security system,
• Pregnant women
• Persons under guardianship or curatorship
• Persons deprived of liberty by a judicial or administrative decision
• Persons who are participating in another clinical study

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Factorial Assignment

Masking: None (Open label)

---

34 participants in 2 patient groups

Control group

Active Comparator group

Description:

Eighteen healthy subjects and eighteen hypertensive patients (men and women) will be enrolled. A 1.5 Tesla MRI device with a large magnet bore (70 cm) will be used, allowing positions change. Two measures will be performed, one in supine position and the other in head down position (-20°). A 3D FSE ASL sequence will be acquired and Cerebral Blood Flow (CBF) maps will be reconstructed. Volume of interest (VOI) will be placed on cortical grey matter (frontal and posterior gyrus), on subcortical deep grey matter (caudate nuclei, thalami) and subcortical white matter (semi oval centers). Differences in CBF values (in mL/100g/min) will be analyzed using SAS 9.3 software for Windows (SAS Institute, Cary North Carolina, USA).

Treatment:

Procedure: MRI

Stroke patients

Active Comparator group

Description:

Eighteen stroke patients (men and women) will be enrolled. A 1.5 Tesla MRI device with a large magnet bore (70 cm) will be used, allowing positions change. Two measures will be performed, one in supine position and the other in head down position (-20°). A 3D FSE ASL sequence will be acquired and Cerebral Blood Flow (CBF) maps will be reconstructed. Volume of interest (VOI) will be placed on cortical grey matter (frontal and posterior gyrus), on subcortical deep grey matter (caudate nuclei, thalami) and subcortical white matter (semi oval centers). Differences in CBF values (in mL/100g/min) will be analyzed using SAS 9.3 software for Windows (SAS Institute, Cary North Carolina, USA).

Treatment:

Procedure: MRI