The Role of Deep Cerebral Vein Variation in Patients With Angiographic Negative Subarachnoid Hemorrhage
1 other identifier
observational
296
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2013
CompletedFirst Submitted
Initial submission to the registry
June 18, 2021
CompletedFirst Posted
Study publicly available on registry
June 28, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2023
CompletedJune 28, 2021
June 1, 2021
10 years
June 18, 2021
June 18, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
favorable or poor outcome
poor outcome (mRS 2-6) or favorable outcome (mRS 0-1).
1 year
Interventions
administered nimodipine to prevent vasospasm, and euvolemia was maintained via intravenous hydration
Eligibility Criteria
This project plans to include 296 patients who meet the admission and discharge criteria
You may qualify if:
- Patients with negative subarachnoid hemorrhage diagnosed by DSA
You may not qualify if:
- In patients with aneurysms, external ventricular drainage (EVD) alone or decompression craniotomy alone or conservative treatment was performed
- Have a history of trauma or prior brain injury (stroke, cerebral hemorrhage, etc., with associated chronic changes on CT)
- Patients with loss of imaging data and severe comorditions prior to onset of SAH
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
2ndAffiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, 310009, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yuanjian Fang, MD
2ndAffiliated Hospital, School of Medicine, Zhejiang University, China
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 18, 2021
First Posted
June 28, 2021
Study Start
January 1, 2013
Primary Completion
January 1, 2023
Study Completion
January 1, 2023
Last Updated
June 28, 2021
Record last verified: 2021-06
Data Sharing
- IPD Sharing
- Will not share