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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05696639
Other study ID # BYL20220216
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date April 1, 2017
Est. completion date December 30, 2023

Study information

Verified date January 2023
Source Shenzhen Baoan District People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cerebral swelling is a major complication following aneurysmal subarachnoid hemorrhage.This study is a retrospective cohort aimed to predict the extent of brain swelling. Cerebral venous assessment can identify the risk of brain swelling and improve surgical outcomes.


Description:

Cerebral swelling is a major complication following aneurysmal subarachnoid hemorrhage (SAH).This study is a retrospective cohort aimed to predict the extent of brain swelling (BS). Cerebral venous assessment can identify the risk of cerebral swelling and improve surgical outcomes. This study is a retrospective cohort analysis. Cerebral venous angiography (CVA) will be adopted and the superficial middle cerebral vein (SMCVs) will be evaluated.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 198
Est. completion date December 30, 2023
Est. primary completion date December 1, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: patients with anterior communicating aneurysm Exclusion Criteria: Hunt-Hess grade I- patients with posterior communicating aneurysm, poor general condition or combined with pregnancy , malignant tumors were excluded.

Study Design


Intervention

Procedure:
Aneurysm embolization
All patients underwent Aneurysm embolization surgery, the cerebral venous will be observed intraoperatively.

Locations

Country Name City State
China Shenzhen Baoan People's Hospital Shenzhen Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Shenzhen Baoan District People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary brain swelling grading of brain swelling 2 weeks
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