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The effect of combined low-dose methylprednisolone on neurological function and hemodynamics in patients with acute cerebral infarction combined with rheumatoid arthriti

The effect of combined low-dose methylprednisolone on neurological function and hemodynamics in patients with acute cerebral infarction combined with rheumatoid arthriti

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075076
Enrollment
Unknown
Registered
2023-08-24
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Cerebrovascular disease

Interventions

non hormone therapy group:oral aspirin tablets (100mg once a day), Clopidogrel (75mg once a day), Atorvastatin calcium tablets (20mg once a day)
Hormone therapy group:Oral administration of methylprednisolone tablets (4mg once per day) on the basis of the control group

Sponsors

Xi'an Fifth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Comply with the diagnostic criteria for acute ischemic stroke proposed in the 2018 Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke; (2) Meets the diagnostic criteria for RA proposed by the American Rheumatology Society/European Alliance Against Rheumatology (ACR/EULAR) in 2010; (3) Acute cerebral infarction onset time = 7 days; (4) Head MRI examination confirmed the presence of cerebral infarction lesions; (5) Can cooperate with TCD inspection; (6) Color Doppler ultrasound of neck vessels indicates that Stenosis = 50%; (7) The patient or family member signs an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Existence of other rheumatic immune diseases; (2) Presence of cerebral hemorrhage, tumors, trauma, etc; (3) Severe liver and kidney dysfunction, cardiac insufficiency, abnormal coagulation mechanisms, gastrointestinal bleeding, and other diseases occur; (4) The medication needs to be adjusted due to intolerance to methylprednisolone tablets or changes in the condition; (5) Failure to adhere to medication or cooperate with follow-up work.

Design outcomes

Primary

MeasureTime frame
Neurological function assessment;Hemodynamic evaluation;Inflammatory activity indicators of rheumatoid arthritis;

Secondary

MeasureTime frame
Rheumatoid arthritis related inflammatory factors;

Countries

China

Contacts

Public ContactYan Jun

Xi'an Fifth Hospital

263329976@qq.com+86 135 7203 4346

Outcome results

None listed

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