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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01567449
Other study ID # 110011
Secondary ID
Status Unknown status
Phase N/A
First received March 25, 2012
Last updated March 28, 2012
Start date September 2011
Est. completion date April 2012

Study information

Verified date March 2012
Source Fujian Medical University
Contact qingsong lin, master
Phone 13489991226
Email lqs1210305061@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to examine the risk factors for aneurysm rebleeding.


Description:

To investigate risk factors for spontaneous aneurysm rebleeding during hospitalization and to reach conclusions if any,of clinical signs for predicting rebleeding.


Recruitment information / eligibility

Status Unknown status
Enrollment 66
Est. completion date April 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Individual whose clinical course was clear enough to be traced back and whose conservative treatment duration was shorter than 6 weeks was included

Exclusion Criteria:

- Rebleeding patients with certain inducing factors such as:

- severe emotional episode,

- severe coughing,

- constipation,

- excessive activities, or

- with coagulation disorder,or

- with other intracranial vascular malformations,such as:

- moyamoya disease,

- arteriovenous malformation were excluded.

- Also patients who rebled while angiography were excluded.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China First Affiliated Hospital,Fujian Medical University Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
Fujian Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Aneurysm rebleeding up to 7 months
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