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Observation on the protective effect of butylphthalide on the blood - brain barrier after stroke in patients with thrombolysis

Observation on the protective effect of butylphthalide on the blood - brain barrier after stroke in patients with thrombolysis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015325
Enrollment
Unknown
Registered
2018-03-23
Start date
2018-04-01
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Cerebrovascular disease

Interventions

test group:rt-PA and Butylphthalide
Control group:Standard dose alteplase treatment

Sponsors

Department of Neurology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) aged 18-80 years old; 2) clinically diagnosed as acute ischemic stroke, NIHSS score 5 or more, the initial onset or previous history of ischemic stroke but no obvious complications; 3) head CT scan showed no cerebral hemorrhage; 4) the patient is eligible for thrombolytic therapy and the patient or family member agrees to have a venous thrombolytic treatment and sign an informed consent form; 5) patients receiving intravenous thrombolysis within the prescribed treatment time window; 6) agree and sign informed consent for clinical use; 7) The patients and their families can cope with the collection, preservation and follow-up of medical history data.

Exclusion criteria

Exclusion criteria: 1) Pre-existing severe liver and kidney dysfunction, cardiac dysfunction, peripheral blood disease, or suffering from other serious systemic diseases; 2) intracerebral hemorrhagic diseases seen by head CT / MRI: cerebral hemorrhage, subarachnoid hemorrhage (excluding pseudo-subarachnoid hemorrhage), etc., or diseases with hemorrhagic tendency; 3) concurrent malignant tumor or ongoing anti-tumor treatment; 4) previous history of allergy to celery or nipop; 5) Pregnancy, lactation or pregnancy may be pregnant and plan patients; 6) Participate in other interventional clinical studies or participate in other interventional clinical studies within 3 months prior to the acquisition date of informed consent; 7) Patients that researchers think are not suitable for this clinical study

Design outcomes

Primary

MeasureTime frame
NIHSS score;mRS score three months after thrombolysis;CT perfusion parameters (including CBV, CBF, PS, MTT);Serological inflammation and tight junction protein indicators: MMP-2, MMP-9, TIMP-1;

Countries

China

Contacts

Public ContactLiang Zhigang

Department of Neurology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University

zgliang@hotmail.com+86 13723987720

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026