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The Safety and Efficacy of Peri-procedure Blood Pressure Management of Revascularization

The Safety and Efficacy of Peri-procedure Blood Pressure Management of Revascularization for Ischemic Cerebral Vascular Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03256513
Enrollment
2270
Registered
2017-08-22
Start date
2017-04-10
Completion date
2019-06-01
Last updated
2017-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Revascularization, Ischemic Cerebrovascular Disease

Brief summary

Objective: Referring The relation between CEA(Carotid endarterectomy) postoperative blood flow monitoring and blood pressure, and combining patient demographics and preoperative risk factors to establish an applicable individual blood pressure controlling model. By comparing with routine antihypertensive strategies through prospective randomized controlled trials , to provide the best perioperative blood pressure control standards and strategies for each patient ,thus better ensuring the safety and efficacy of CEA .

Interventions

OTHERmodel controlling

control blood pressure by statistical l model with anticipate lowest peri-procedure risk

OTHERconventional controlling

control blood pressure by conventional strategy

Sponsors

Beijing Tiantan Hospital
CollaboratorOTHER
Peking University Third Hospital
CollaboratorOTHER
The 306 Hospital of People's Liberation Army
CollaboratorOTHER
Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* symptomatic patient with carotid artery stenosis\>=50% or asymptomatic patient with carotid artery stenosis\>=70%, according to DSA or CTA; * without massive cerebral infarction(infarction area \>1/2 territory of middle cerebral artery) confirmed by CT or MRI; * informed consent acquired.

Exclusion criteria

* lesion beyond range limit of procedure (higher than C2); * target vascular complete occlusion or ipsilateral intracranial artery severe stenosis or complete occlusion cannot be revascularized via CEA procedure * nonatherosclerotic carotid stenosis, such as vasculitis, dissection, congenital vascular malformation; * history of instable angina pectoris, myocardial infarction or congestive heart failure within 6 months unable to accept systematic anesthesia; * history of severe injury, surgery or radiotherapy on neck; * with comorbid hemorrhagic cerebral disease such as intracranial aneurysm or vascular malformation; * with comorbid blood system disease causing refractory coagulation dysfunction or rejection to blood or blood products perfusion; * with other comorbidity, expected life \< 2 years; * severe diabetes mellitus difficult to control, blood sugar \>300mg/dl; * pregnancy or peri-natal period; * intolerance to systematic anesthesia or surgery after adequate preparation. * intolerance to peri-procedural drug possible to administrated; * not cooperating or rejecting to informed consent;

Design outcomes

Primary

MeasureTime frameDescription
death30 daysall cause death
ischemic stroke30 daysIschemic stroke is defined as an acute episode of neurological events with focal symptoms and signs, with a duration of more than 24h and confirmed by imaging.
cardiovascular events30 daysCardiovascular events were defined as: ECG presentation clearly different from preoperative myocardial ischemia, myocardial infarction, arrhythmia and cardiovascular death.

Secondary

MeasureTime frameDescription
transient ischemic attack,TIA30 daystransient ischemic attack, TIA is defined as: Patients with new onset of neurological symptoms and / or signs, duration \< 24 hours, MRI diffusion weighted imaging (DWI) did not find new infarcts. If MRI DWI showed new lesion, ischemic stroke was defined.
epilepsy30 daysepilepsy is defined as focal onset, with or without evolution to a bilateral tonic-clonic seizure, confirmed by EEG findings including interictal epileptiform discharges (IEDs), lateralized periodic discharges (LPDs; previously known as periodic lateralized epileptiform discharges \[PLEDs\]), and generalized periodic discharges (GPDs)
cerebral hemorrhage30 dayscerebral hemorrhage including intracerebral hemorrhage, epidural or subdural hemorrhage, subarachnoid hemorrhage.
hyperperfusion syndrome30 daysHyperfusion Syndrome is defined as : 30 days after operation, new onset headache, vomiting, mental symptoms, macular edema, focal seizures, neurological dysfunction, or imaging brain edema, visible bleeding, and exception of new ischemic cerebral infarction or other causes.

Countries

China

Contacts

Primary ContactLiqun Jiao, MD
jiaoliqun@gmail.com86-10-83198899

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026