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Clinical Trial Summary

A randomized, double-blind, placebo-controlled study on the treatment of refractory distributed shock with angiotensin II injection, with a random ratio of 1:1. Assuming a success rate of 25% for the main therapeutic endpoint in the control group and 50% for the experimental group, a total of 214 subjects will be enrolled, including 107 in the experimental group and 107 in the control group.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06351150
Study type Interventional
Source Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Contact Xiangdong Guan, M.D.
Phone 13802925067
Email guanxiangdong1962@163.com
Status Not yet recruiting
Phase Phase 3
Start date May 2024
Completion date December 2027

See also
  Status Clinical Trial Phase
Terminated NCT03378466 - Heparin Anticoagulation in Septic Shock Phase 2
Recruiting NCT05824767 - Serum Biomarkers to Predict Response to Angiotensin II in Septic Shock Phase 4
Approved for marketing NCT03245528 - Expanded Access for LJPC-501 N/A