Skip to content

Clinical Study on the Effects of Plasma Adsorption Therapy on Neurological Function and Inflammatory Factors in Patients with Ischemic Stroke

Clinical Study on the Effects of Plasma Adsorption Therapy on Neurological Function and Inflammatory Factors in Patients with Ischemic Stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084204
Enrollment
Unknown
Registered
2024-05-12
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Acute Ischemic Stroke

Interventions

Experimental group:Combination therapy of conventional medication with plasma adsorption therapy
Control group:Conventional drug therapy

Sponsors

The Fifth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1: Age = 18 years; 2: Clinically confirmed first-ever acute ischemic stroke, meeting the diagnostic criteria of the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018"; 3: Onset within 72 hours; 4: NIHSS score of 4-22 points; 5: Pre-stroke mRS score = 1 point; 6: Patients with elevated inflammatory factors; 7: Willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1: Patients receiving thrombolytic therapy and/or interventional treatment; 2: Patients with active bleeding or severe bleeding tendencies; 3: Coagulation disorders; 4: Patients with infections, with axillary or ear temperature = 37.5°C; 5: Patients with tumors; 6: Patients with immune system disorders; 7: Pregnant or lactating women; 8: Patients with other conditions that prevent them from undergoing relevant blood purification treatment (such as moderate to severe anemia, hypotension, inability to meet puncture requirements) or those who cannot effectively cooperate; 9: Patients allergic to study drugs or medical devices (extracorporeal circulation, blood perfusion devices); 10: Other conditions judged by the investigator as unsuitable for inclusion; 11: Patients receiving treatment with drugs such as alteplase.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with 90-day mRS Score 0-2;

Secondary

MeasureTime frame
inflammatory factors;0-day cognitive function score MMSE, MoCA;

Countries

China

Contacts

Public ContactLei zhang

The Fifth Affiliated Hospital of Sun Yat-sen University

zhangl92@mail.sysu.edu.cn+86 137 2620 9240

Outcome results

None listed

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