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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04941846
Other study ID # 2020111
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2013
Est. completion date January 2023

Study information

Verified date June 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Jianmin Zhang, MD
Phone +86 13805722695
Email zjm135@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The incidence of Rosenthal basilar vein (BVR) variants (deep venous drainage variants) was relatively increased in patients with AN-SAH compared with patients with aneurysms. However, the inclusion criteria for AN-SAH patients in these studies were different. Some studies have investigated both PAN-SAH and NPAN-SAH, while some studies have only investigated PAN-SAH patients. However, we believe that NPAN-SAH may be the bleeding caused by non-BVR variation. Although previous studies did not find any association between NPAN-SAH and BVR variants, the results in their study were different, which may be due to the limited number of cases.


Recruitment information / eligibility

Status Recruiting
Enrollment 296
Est. completion date January 2023
Est. primary completion date January 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: Patients with negative subarachnoid hemorrhage diagnosed by DSA Exclusion Criteria: 1. In patients with aneurysms, external ventricular drainage (EVD) alone or decompression craniotomy alone or conservative treatment was performed 2. Have a history of trauma or prior brain injury (stroke, cerebral hemorrhage, etc., with associated chronic changes on CT) 3. Patients with loss of imaging data and severe comorditions prior to onset of SAH

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
nimodipine and euvolemia
administered nimodipine to prevent vasospasm, and euvolemia was maintained via intravenous hydration

Locations

Country Name City State
China 2ndAffiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary favorable or poor outcome poor outcome (mRS 2-6) or favorable outcome (mRS 0-1). 1 year
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