Table of contents
- Trial overview
- Acute kidney injury study after cardiac surgery
- Liver cancer radioembolization study
- Pediatric shock and low blood pressure study
- Main outcomes and what they mean
- Who the trials are for
- Study phases and current status
Trial overview
The data include three interventional studies of ANGIOTENSIN II, each looking at a different clinical problem: kidney injury after heart surgery, liver cancer treatment, and severe low blood pressure in children.[1][2][3]
All three studies are marked Authorised, which means they have been approved to move forward in the study process.[1][2][3]
Acute kidney injury study after cardiac surgery
Trial NCT06615102 is studying whether ANGIOTENSIN II can reduce the occurrence of acute kidney injury after cardiac surgery.[1] The trial compares ANGIOTENSIN II with norepinephrine, another blood pressure medicine, in people after heart surgery.[1]
The main outcome is the rate of AKI KDIGO stage 2 or 3, or death, within 72 hours after surgery.[1] KDIGO is a kidney injury staging system; stage 2 or 3 means a more serious level of kidney injury.[1]
This study is large, with an enrollment of 1022 people, and it is listed as Low Intervention in the source data.[1]
Liver cancer radioembolization study
Trial 2025-521870-33-00 is called the RADIANT study and is testing ANGIOTENSIN II in people with primary or secondary liver cancer.[2] The study looks at whether ANGIOTENSIN II can make radioembolization more effective.[2]
Radioembolization is a cancer treatment that delivers tiny radioactive microspheres into the blood supply of the tumor.[2] In this study, the main measure is the tumor-to-non-tumor ratio, which compares how much treatment reaches the tumor versus nearby normal tissue.[2]
The trial uses imaging tests called 90Y PET/CT and 99mTc-MAA SPECT/CT to compare results with and without ANGIOTENSIN II.[2] It is a small Phase 2 study with 15 participants.[2]
Pediatric shock and low blood pressure study
Trial 2025-523750-14-00 is studying ANGIOTENSIN II in patients 0 to 17 years old who have refractory hypotension in distributive shock.[3] Refractory hypotension means blood pressure that stays too low even after usual treatment.[3]
The study compares ANGIOTENSIN II with placebo while children receive fluids and standard-of-care vasopressors.[3] A placebo is a treatment with no active medicine, used here to help compare results fairly.[3]
The main outcome is the change in the dose of standard blood pressure medicines, measured as norepinephrine base equivalent dose, during the first 6 hours of treatment.[3] This Phase 3 trial includes 143 participants.[3]
Main outcomes and what they mean
The kidney study focuses on whether serious kidney injury or death happens within 72 hours after cardiac surgery.[1]
The liver cancer study focuses on whether ANGIOTENSIN II improves the tumor-to-non-tumor ratio after treatment, which may show better targeting of the tumor area.[2]
The pediatric shock study focuses on whether ANGIOTENSIN II can reduce the amount of standard blood pressure medicine needed in the first 6 hours.[3]
Who the trials are for
These studies are not for one single disease group; they are designed for very different patients.[1][2][3]
The first study is for people after cardiac surgery who are at risk of acute kidney injury.[1]
The second study is for people with primary or secondary liver cancer.[2]
The third study is for children and teenagers from 0 to 17 years old with refractory hypotension in distributive shock.[3]
Study phases and current status
The source data show one Phase 2 study, one Phase 3 study, and one study labeled Low Intervention.[1][2][3]
Phase 2 studies usually look more closely at whether a treatment seems to work and how it performs in a smaller group, while Phase 3 studies compare treatments in larger groups to confirm results.[2][3]
All three studies are marked Authorised, and their enrollment ranges from 15 to 1022 participants.[1][2][3]





