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Effect and Safety Study of Atorvastatin to Treat Chronic Subdural Hematoma

Chronic Subdural Hematoma Clinical Trial

Official title:
Multi-Center, Randomized, Placebo-Controlled, Double Blind Study of the Atorvastatin: Effect on Patients With Chronic Subdural Hematoma

Clinical Trial Summary

To evaluate the clinic effects and security of oral administration of Atorvastatin on chronic subdural hematoma (CSDH).

Clinical Trial Description

Study design:

Multi-center, randomized, double-blind, placebo parallel controlled

Subjects:

Patients with chronic subdural hematoma (CSDH)

Sample size:

200, including an Atorvastatin-treated group of 100 patients and a control group of 100 subjects. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02024373
Study type Interventional
Source Oriental Neurosurgery Evidence-Based-Study Team
Contact
Status Completed
Phase Phase 2
Start date December 2013
Completion date September 2016
View Details
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