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TCD Monitoring Technology Guides the Precise Control of Blood Pressure After EVT

TCD Monitoring Technology Guides the Precise Control of Blood Pressure After EVT

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03529149
Enrollment
90
Registered
2018-05-18
Start date
2018-04-08
Completion date
2019-06-01
Last updated
2018-05-18

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

Conditions

Acute Ischemic Stroke

Brief summary

Investigators hypothesized that the precise regulation of blood pressure based on the changes of cerebral blood flow parameters under TCD monitoring can better improve the state of cerebral blood flow, reduce the risk of early neurological deterioration and improve the prognosis of the patients.

Interventions

Accurate monitoring of blood pressure is carried out under TCD monitoring, that is to maintain (mean flow velocity)MFV or (pulse index)PI target blood pressure. The target values of MFV and PI are MFV\>37cm/s of (middle cerebral artery)MCA, PI \< 1.34cm/s, aMFV\>40cm/s of (basilar artery)BA, PI \< 0.8cm/s. TCD shows that when the MFV of MCA or BA is lower than the target value, the blood pressure is reduced or discontinued according to the insufficiency of blood flow. and the current blood pressure is maintained once MFV is met. TCD showed that the PI index of MCA or BA was higher than the target value . The blood pressure reduction was treated by excessive perfusion: intravenous infusion of blood pressure drugs , once PI index is up to the standard, maintaining the current blood pressure.

Sponsors

Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* 18 years of age or older; * accept EVT treatment within 6 hours of symptoms onset; * In selected patients with AIS within 6 to 16 hours of last known normal who have LVO in the anterior circulation and meet other DAWN or DEFUSE 3 eligibility criteria.. * In selected patients with AIS within 6 to 24 hours of last known normal who have LVO in the anterior circulation and meet other DAWN eligibility criteria.

Exclusion criteria

* Pre - onset mRS\>2; * severe dementia; * threatening life diseases (such as malignant tumor, etc.); * non acute ischemic cerebrovascular disease patients undergoing selective intravascular treatment; * related sound window closure can not be monitoring with TCD.

Design outcomes

Primary

MeasureTime frameDescription
early neurological deterioration72 hoursthe incidence of 72 hours in National Institute of Health stroke scale increased more than 4 points or National Institute of Health stroke scale Ia score more than 1 points

Secondary

MeasureTime frameDescription
prognosis of nerve function3 monthsprognosis of nerve function use Modified Rankin Scale,0\ 3 is good prognosis and 4\ 6 is poor prognosis.

Countries

China

Outcome results

None listed

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