Condition: Abirritation in the ICU · Sponsor: Jiangsu HengRui Medicine Co., Ltd.
The purpose of this study is to evaluate the efficacy and safety of Tegileridine Fumarate lnjection for prolonged abirritation(48h to 72h) during mechanical ventilation in the ICU.
This description comes directly from the study's public registry record.
Lei Tang · +0518-82342973 · ei.tang.lt31@hengrui.com
Always discuss trial participation with your own doctor first.
| Zhongshan Hospital | Shanghai, Shanghai Municipality, China | Recruiting |
| Union Hospital, Tongji Medical College, Huazhong University of Science and Technology | Hubei, Wuhan, China | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07372924