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Nalmefene improves prognosis in patients with a large cerebral infarction

Nalmefene improves prognosis in patients with a large cerebral infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013871
Enrollment
Unknown
Registered
2017-12-12
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-12-18

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

Conditions

large cerebral infarction

Interventions

1:conventional dehydration
2:Be intravenously administered 0.2 mg nalmefene hydrochloride injection

Sponsors

the First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnostic criteria of cerebral infarction caused by occlusion of the middle cerebral artery trunk according to the Fourth National Academic Conference on the Diagnosis of Cerebrovascular Disease,and confirmed by CT and/or MRI of the head; 2. Onset time = 3d; 3. First onset; 4. Aged 18-80 years; 5. Provision of wirtten informed consent by patients relatives or legal surrogate.

Exclusion criteria

Exclusion criteria: 1. Receive arterial thrombolysis treatment before treatment; 2. Presence of new infarcts or incidence of hemorrhagic infarct during the process of treatment; 3. Severe damage to other organs; 4. With cognitive disorder, neuropsychiatric disorder, drug abuse or alcoholism; 5. Recently taken or are taking immunosuppressive drugs; 6. Maligant tumor; 7. Pregnant or lactating woman; 8. Participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
effective rate;

Secondary

MeasureTime frame
NIHSS score;GCS;Serum level of MMP-9 at;MRI perfusion imaging of the head;

Countries

China

Contacts

Public ContactHou Weichen

the First Hospital of Jilin University

48580116@qq.com+86 13504308263

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026