Lai Xinxing, Xiong Xuejiao, Jia Qi, Liu Tingting, Yang Zhaowen, Zhang Chi, Kong Lingbo, Cao Kegang, Dong Ting, Fang Caixia, Ge Jianwen, Dong Li, Zong Zhitao, Chen Sisi, Ma Yuhong, Bai Xue, Wu Dahua, Xie Yao, Zhang Mingyan, Wang Yilong, Jiang Guohui, Song Daqiao, Wang Yanping, Gui Chunyan, Geng Qingwen, Gao Ying
Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Institute for Brain Disorders, Beijing University of Chinese Medicine, Beijing, China.
BMC Complement Med Ther. 2025 Jan 28;25(1):30. doi: 10.1186/s12906-025-04762-9.
Suhexiang (SHX) pill is widely used for treating acute ischemic stroke (AIS). Experimental and randomized controlled trials suggested that SHX pill was beneficial for patients with AIS. However, the effectiveness of SHX pill in real-world practice setting remains unclear. It is of great importance to investigate the effectiveness and safety of SHX pill in patients with acute ischemic stroke in real-world clinical practice with long-term follow-up.
The Suhexiang pill for acute ischemic stroke in Real-world Practice Setting (SUNRISE) is a multicenter, prospective, product-specific, observational study designed to provide insight into the administration of SHX pill for patients with AIS in the real-world clinical practice setting, with an initial sample size of 1000. Eligible patients treated with SHX pill within seven days of AIS onset will be consecutively included in this registry. The primary outcome is the proportion of patients independent at 3 months after stroke onset defined by an mRS score of 0, 1, or 2.
The findings of the SUNRISE registry will not only provide insights into the characteristics of patients who may benefit from SHX treatment, but also may enable the individualized treatment decision-making of SHX pill in real-world practice setting.
This study was registered with the ClinicalTrials.gov (URL: https://clinicaltrials.gov/ , Unique identifier: NCT05833932).
苏合香丸广泛用于治疗急性缺血性卒中(AIS)。实验研究和随机对照试验表明,苏合香丸对AIS患者有益。然而,苏合香丸在实际临床环境中的有效性仍不明确。在真实世界临床实践中对急性缺血性卒中患者长期随访,研究苏合香丸的有效性和安全性具有重要意义。
“真实世界实践环境中苏合香丸治疗急性缺血性卒中(SUNRISE)”研究是一项多中心、前瞻性、针对特定产品的观察性研究,旨在深入了解苏合香丸在真实世界临床实践中对AIS患者的应用情况,初始样本量为1000例。符合条件的在AIS发病7天内接受苏合香丸治疗的患者将被连续纳入该登记研究。主要结局是卒中发病3个月后改良Rankin量表(mRS)评分为0、1或2定义的独立患者比例。
SUNRISE登记研究的结果不仅将深入了解可能从苏合香丸治疗中获益的患者特征,还可能在真实世界实践环境中实现苏合香丸的个体化治疗决策。
本研究已在ClinicalTrials.gov注册(网址:https://clinicaltrials.gov/ ,唯一标识符:NCT05833932)。