Examining the role of the cerebral venous system in stroke patients receiving reperfusion therapy
Study of the Function of Cerebral Venous System in Acute Ischemic Stroke Patients Receiving Reperfusion Therapy
This study is testing how the veins in the brain affect recovery in stroke patients who receive treatment to restore blood flow within 24 hours of their symptoms starting.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University Academic / other |
| Locations | 1 site (Hangzhou, Zhejiang) |
| Trial ID | NCT03838289 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on patients with acute ischemic stroke who receive reperfusion therapy within 24 hours of symptom onset. Participants undergo neurological examinations and advanced imaging techniques, including multimodal computed tomography and magnetic resonance perfusion, to evaluate various brain parameters. The study aims to investigate the status of the cerebral venous system and its potential impact on patient outcomes following reperfusion therapy. By analyzing venous markers, the researchers hope to identify reliable predictors of prognosis for these patients.
Who should consider this trial
Good fit: Ideal candidates are individuals diagnosed with acute ischemic stroke who can receive reperfusion therapy within 24 hours of onset.
Not a fit: Patients with contraindications to imaging with contrast agents or those unable to provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved prognostic markers for stroke patients, enhancing treatment strategies and outcomes.
How similar studies have performed: While the role of arterial collaterals has been studied, the specific focus on the cerebral venous system in this context is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. receive reperfusion therapy within 24 hours after onset; 2. undergo multimodal magnetic resonance computed tomography before reperfusion therapy and CTP or magnetic resonance perfusion at 24 hours after reperfusion therapy; Exclusion Criteria: 1. Contraindication to imaging with contrast agents; 2. Without provision of informed consent.
Where this trial is running
Hangzhou, Zhejiang
- The second affiliated hosipital of Zhejiang University — Hangzhou, Zhejiang, China (Recruiting)
Study contacts
- Study coordinator: Min Lou, Ph.D
- Email: loumingxc@vip.sina.com
- Phone: 13958007213
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.