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Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial
BACKGROUND: Chronic 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 t...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652431/ https://www.ncbi.nlm.nih.gov/pubmed/26581842 http://dx.doi.org/10.1186/s13063-015-1045-y |
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author | Jiang, Rongcai Wang, Dong Poon, Wai Sang Lu, Yi Cheng Li, Xin Gang Zhao, Shi Guang Wang, Ren Zhi You, Chao Yuan, Xian Rui Zhang, Jian Min Feng, Hua Fei, Zhou Yu, Xin Guang Zhao, Yuan Li Hu, Jin Kang, De Zhi Yu, Ru Tong Gao, Guo Dong De Zhu, Xi Sun, Tao Hao, Jie He Liu, Xian Zhi Su, Ning Yue, Shu Yuan Zhang, Jian Ning |
author_facet | Jiang, Rongcai Wang, Dong Poon, Wai Sang Lu, Yi Cheng Li, Xin Gang Zhao, Shi Guang Wang, Ren Zhi You, Chao Yuan, Xian Rui Zhang, Jian Min Feng, Hua Fei, Zhou Yu, Xin Guang Zhao, Yuan Li Hu, Jin Kang, De Zhi Yu, Ru Tong Gao, Guo Dong De Zhu, Xi Sun, Tao Hao, Jie He Liu, Xian Zhi Su, Ning Yue, Shu Yuan Zhang, Jian Ning |
author_sort | Jiang, Rongcai |
collection | PubMed |
description | BACKGROUND: Chronic 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/DESIGN: We 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 4(th), 12(th), and 24(th) 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. DISCUSSION: Results of this trial will provide critical information regarding whether atorvastatin is an effective and safe alternative to surgical treatment of CSDH. TRIAL REGISTRATION: ClinicalTrials.gov Identifier – NCT02024373 The date of trial registration: 7 August 2013 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-015-1045-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4652431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46524312015-11-20 Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial Jiang, Rongcai Wang, Dong Poon, Wai Sang Lu, Yi Cheng Li, Xin Gang Zhao, Shi Guang Wang, Ren Zhi You, Chao Yuan, Xian Rui Zhang, Jian Min Feng, Hua Fei, Zhou Yu, Xin Guang Zhao, Yuan Li Hu, Jin Kang, De Zhi Yu, Ru Tong Gao, Guo Dong De Zhu, Xi Sun, Tao Hao, Jie He Liu, Xian Zhi Su, Ning Yue, Shu Yuan Zhang, Jian Ning Trials Study Protocol BACKGROUND: Chronic 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/DESIGN: We 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 4(th), 12(th), and 24(th) 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. DISCUSSION: Results of this trial will provide critical information regarding whether atorvastatin is an effective and safe alternative to surgical treatment of CSDH. TRIAL REGISTRATION: ClinicalTrials.gov Identifier – NCT02024373 The date of trial registration: 7 August 2013 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-015-1045-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-18 /pmc/articles/PMC4652431/ /pubmed/26581842 http://dx.doi.org/10.1186/s13063-015-1045-y Text en © Jiang et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Jiang, Rongcai Wang, Dong Poon, Wai Sang Lu, Yi Cheng Li, Xin Gang Zhao, Shi Guang Wang, Ren Zhi You, Chao Yuan, Xian Rui Zhang, Jian Min Feng, Hua Fei, Zhou Yu, Xin Guang Zhao, Yuan Li Hu, Jin Kang, De Zhi Yu, Ru Tong Gao, Guo Dong De Zhu, Xi Sun, Tao Hao, Jie He Liu, Xian Zhi Su, Ning Yue, Shu Yuan Zhang, Jian Ning Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title | Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title_full | Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title_fullStr | Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title_full_unstemmed | Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title_short | Effect of ATorvastatin On Chronic subdural Hematoma (ATOCH): a study protocol for a randomized controlled trial |
title_sort | effect of atorvastatin on chronic subdural hematoma (atoch): a study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652431/ https://www.ncbi.nlm.nih.gov/pubmed/26581842 http://dx.doi.org/10.1186/s13063-015-1045-y |
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