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How can we improve the bloof flow in the brain during bypass surgery of the brain?

Phase 1
Conditions
Patients with an indication for an extracranial-intracanial bypass (e.g. Moya Moya Disease, occluded carotid artery, giant aneurysm)
MedDRA version: 20.0Level: LLTClassification code 10029999Term: Occlusion carotidSystem Organ Class: 100000004852
MedDRA version: 20.1Level: LLTClassification code 10002333Term: Aneurysm cerebralSystem Organ Class: 100000004852
MedDRA version: 20.1Level: LLTClassification code 10002337Term: Aneurysm intracranialSystem Organ Class: 100000004852
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
Registration Number
EUCTR2018-002008-15-NL
Lead Sponsor
niversity Medical Center Utrecht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Adults, aged 18 years or above
Indication for extracranial-intracranial bypass surgery
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 8
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 2

Exclusion Criteria

Patients within two weeks after a subarachnoid hemorrhage
Language barrier
Pregnancy
Hypertrophic cardiomyopathy
Left ventricular outflow tract obstruction
Severe, untreated, ventricular arrhytmia
Severe hyperthyroidism
Recent myocardial infarction (<30days) or unstable angina
Hypersensitivity for dobutamine or phenylephrine
Mean arterial blood pressure < 60 mmHg under general anesthesia before start of the study period
Systolic blood pressure > 180 mmHg under general anesthesia before start of the study period

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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