Cargando…
Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II)
BACKGROUND: Hypertensive intracerebral haemorrhage (HICH), which is characterized by rapid change, high morbidity, and mortality, is extremely dangerous. Both medical and surgical treatments lack definitive evidence and remain controversial. A prospective RCT that we have conducted has shown that th...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129335/ https://www.ncbi.nlm.nih.gov/pubmed/30224926 http://dx.doi.org/10.1155/2018/3120179 |
_version_ | 1783353784517263360 |
---|---|
author | Zhang, Qixin Zeng, Liling Chen, Xiuyan Zhou, Yuexiang Gong, Baoying Li, Haijun Guo, Jianwen |
author_facet | Zhang, Qixin Zeng, Liling Chen, Xiuyan Zhou, Yuexiang Gong, Baoying Li, Haijun Guo, Jianwen |
author_sort | Zhang, Qixin |
collection | PubMed |
description | BACKGROUND: Hypertensive intracerebral haemorrhage (HICH), which is characterized by rapid change, high morbidity, and mortality, is extremely dangerous. Both medical and surgical treatments lack definitive evidence and remain controversial. A prospective RCT that we have conducted has shown that the usage of the herbal medicine ICH-012 within 6 h of the event may increase the risk of haematoma enlargement and gastrointestinal bleeding. However, the volume of haematoma remains stable after 6 h. Thus, we will increase the time window to the period from 6 to 72 h after onset to evaluate the safety and efficacy of ICH-012 treating ICH (ClinicalTrial.gov ID: NCT03354026). METHODS/DESIGN: The CRRICHTrial-II study, a prospective, double-blinded, controlled, multicentre RCT, includes three groups: A, B, and C. Group A patients were treated with 8 herbal medicines (with 2 herbal medicines of Hirudo and Tabanus as well as 6 other combined herbal medicines of Group B) and Group C were placebo. Patients should meet all the inclusion criteria: age between 18 and 80 and diagnosis of HICH by brain CT scan between 6 and 72 h from the onset. The CT scan will be taken at four critical time points: baseline, between 6 and 72h, 24h after onset, and between 10 and 14 days after onset. The drug intervention lasts 10 days, and there is a follow-up visit taken after 90 days. The haematoma enlargement after 24 h onset as demonstrated by CT is the primary outcome. DISCUSSION: A large amount of data from high-quality RCTs is needed for the extensive clinical application of herbal medicine. The CRRICHTrial-II will evaluate the safety and effectiveness of ICH-012 in a safer time window between 6 and 72 h and investigate the possible mechanisms of action and direction of herbal medicine in the haematoma growth after HICH. Trial registration at ClinicalTrial.gov, ID: NCT03354026, is registered on 23rd Nov. 2017. |
format | Online Article Text |
id | pubmed-6129335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-61293352018-09-17 Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) Zhang, Qixin Zeng, Liling Chen, Xiuyan Zhou, Yuexiang Gong, Baoying Li, Haijun Guo, Jianwen Evid Based Complement Alternat Med Research Article BACKGROUND: Hypertensive intracerebral haemorrhage (HICH), which is characterized by rapid change, high morbidity, and mortality, is extremely dangerous. Both medical and surgical treatments lack definitive evidence and remain controversial. A prospective RCT that we have conducted has shown that the usage of the herbal medicine ICH-012 within 6 h of the event may increase the risk of haematoma enlargement and gastrointestinal bleeding. However, the volume of haematoma remains stable after 6 h. Thus, we will increase the time window to the period from 6 to 72 h after onset to evaluate the safety and efficacy of ICH-012 treating ICH (ClinicalTrial.gov ID: NCT03354026). METHODS/DESIGN: The CRRICHTrial-II study, a prospective, double-blinded, controlled, multicentre RCT, includes three groups: A, B, and C. Group A patients were treated with 8 herbal medicines (with 2 herbal medicines of Hirudo and Tabanus as well as 6 other combined herbal medicines of Group B) and Group C were placebo. Patients should meet all the inclusion criteria: age between 18 and 80 and diagnosis of HICH by brain CT scan between 6 and 72 h from the onset. The CT scan will be taken at four critical time points: baseline, between 6 and 72h, 24h after onset, and between 10 and 14 days after onset. The drug intervention lasts 10 days, and there is a follow-up visit taken after 90 days. The haematoma enlargement after 24 h onset as demonstrated by CT is the primary outcome. DISCUSSION: A large amount of data from high-quality RCTs is needed for the extensive clinical application of herbal medicine. The CRRICHTrial-II will evaluate the safety and effectiveness of ICH-012 in a safer time window between 6 and 72 h and investigate the possible mechanisms of action and direction of herbal medicine in the haematoma growth after HICH. Trial registration at ClinicalTrial.gov, ID: NCT03354026, is registered on 23rd Nov. 2017. Hindawi 2018-08-26 /pmc/articles/PMC6129335/ /pubmed/30224926 http://dx.doi.org/10.1155/2018/3120179 Text en Copyright © 2018 Qixin Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Qixin Zeng, Liling Chen, Xiuyan Zhou, Yuexiang Gong, Baoying Li, Haijun Guo, Jianwen Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title | Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title_full | Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title_fullStr | Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title_full_unstemmed | Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title_short | Clinical Evaluation of Herbal Medicine (ICH-012) in Treating Acute Cerebral Haemorrhage: Safety and Efficacy from 6- to 72-Hour Time Window (CRRICHTrial-II) |
title_sort | clinical evaluation of herbal medicine (ich-012) in treating acute cerebral haemorrhage: safety and efficacy from 6- to 72-hour time window (crrichtrial-ii) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129335/ https://www.ncbi.nlm.nih.gov/pubmed/30224926 http://dx.doi.org/10.1155/2018/3120179 |
work_keys_str_mv | AT zhangqixin clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT zengliling clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT chenxiuyan clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT zhouyuexiang clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT gongbaoying clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT lihaijun clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii AT guojianwen clinicalevaluationofherbalmedicineich012intreatingacutecerebralhaemorrhagesafetyandefficacyfrom6to72hourtimewindowcrrichtrialii |