Abstract

BackgroundChronic subdural hematoma (CSDH) is a common disease that is more prevalent in older people. Surgical intervention is a safe treatment of choice. However, the recurrence rate is relatively high and the outcome is not always satisfactory among surgically treated patients. It is believed that aberrant angiogenesis and intracapsular inflammation contribute to the development of CSDH. Atorvastatin is reported to promote angiogenesis and suppress inflammation. We have recently shown that atorvastatin is effective to non-surgically reduce and eliminate CSDH with minimal side effects. Here, we report a clinical research trial protocol that is designed to evaluate the therapeutic effects of atorvastatin on CSDH.Methods/DesignWe have designed a multi-center, randomized, placebo-controlled, double blind clinical trial for evaluating the efficacy of oral atorvastatin in reducing CSDH. We have so far recruited 96 patients with CT-confirmed or MRI-confirmed CSDHs from 16 medical centers in China. These patients were originally recruited for the Oriental Neurosurgical Evidence-based Study Team (ONET) study. After informed consent is provided, patients are randomized to receive either atorvastatin (oral 20 mg/night for 8 weeks) or placebo (dextrin for 8 weeks); and followed for 16 weeks after the treatment. The primary outcome is the change in hematoma volume at the end of 8-week treatment. Secondary outcomes include: changes in 1) the hematoma volume at the 4th, 12th, and 24th weeks; 2) Markwalder’s Grading Scale and Glasgow Coma Scale (MGS-GCS); 3) Glasgow Outcome Score (GOS) and 4) Activities of Daily Life – the Barthel Index scale (ADL-BI). Safety will be assessed during the study by monitoring adverse events, laboratory tests, electrocardiography (ECG), measurements of vital signs (temperature, pulse, and blood pressure) and body weight.DiscussionResults of this trial will provide critical information regarding whether atorvastatin is an effective and safe alternative to surgical treatment of CSDH.Trial registrationClinicalTrials.gov Identifier – NCT02024373The date of trial registration: 7 August 2013Electronic supplementary materialThe online version of this article (doi:10.1186/s13063-015-1045-y) contains supplementary material, which is available to authorized users.

Highlights

  • Chronic subdural hematoma (CSDH) is a common disease that is more prevalent in older people

  • Results of this trial will provide critical information regarding whether atorvastatin is an effective and safe alternative to surgical treatment of CSDH

  • ATorvastatin On Chronic subdural Hematoma (ATOCH) is an atorvastatin-based clinical trial for CSDH. It is the first complete conservative treatment trial for CSDH, undertaken in order to exclude the influence of surgery as compared to previous trials focusing on reducing the relapse of CSDH after surgery

Read more

Summary

Discussion

ATOCH is an atorvastatin-based clinical trial for CSDH To our knowledge, it is the first complete conservative treatment trial for CSDH, undertaken in order to exclude the influence of surgery as compared to previous trials focusing on reducing the relapse of CSDH after surgery. We propose to test atorvastatin, but not other statins, based on our published report on treating CSDH with atorvastatin We believe that this trial is necessary because options for conservative treatment of CSDH are very limited [34,35,36]. All authors belong to the Oriental Neurosurgical Evidence-based Study Team (ONET) of People’s Republic of China

Background
Methods/Design
10. Linyi People’s Hospital
14. The First Affiliated Hospital of Harbin Medical University
Findings

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.