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Search / Trial NCT06539234

Angiotensin II Stress Test. Renin Kinetics During Treatment of Vasoplegic Shock With Angiotensin II.

Launched by UNIVERSITY MEDICAL CENTRE MARIBOR · Aug 1, 2024

Trial Information

Current as of August 25, 2025

Recruiting

Keywords

Shock, Distributive Angiotensin Ii Renin Shock, Septic Vasoplegia

ClinConnect Summary

This clinical trial, called the Angiotensin II Stress Test, is studying how a medication called angiotensin II can help patients with a serious condition known as vasoplegic shock. In this type of shock, patients often have very low blood pressure, which can lead to dangerous complications. The trial aims to understand the relationship between a substance called renin, which is involved in blood pressure regulation, and the effectiveness of angiotensin II treatment. Researchers want to find out if measuring renin levels can help identify which patients are most likely to benefit from angiotensin II when other medications haven’t worked.

To be eligible for this trial, participants must be adults with distributive shock that has lasted less than 72 hours and have not responded to standard treatments with noradrenaline and vasopressin. They should also be expected to survive for more than 24 hours and have no serious health issues that would prevent them from participating. If you join the study, you can expect to receive close monitoring and care while researchers gather important information about how angiotensin II and renin levels relate to your treatment and recovery. This study is currently recruiting participants, and it could help improve treatment options for people experiencing this critical condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • patients with distributive shock lasting \< 72 hours
  • a goal mean arterial pressure (65-85 mmHg) not achieved despite an infusion of at least noradrenaline 0.3 mcg/kg/min and vasopressin 0.03 IE/min
  • the patient did not get angiotensin II before
  • predicted survival is \>24h
  • no limitations for active treatment
  • Exclusion Criteria:
  • burns \>20% body area
  • acute coronary syndrome
  • bronchospasm
  • liver disease (MELD ≥30)
  • severe acute bleeding (need for 4 or more units of concentrated erythrocyte)
  • acute mesenteric ischemia
  • aortic dissection
  • leucopenia \<1000/mm3
  • pregnancy
  • Raynaud disease, systemic sclerosis, vasospastic disease
  • the need for daily dose of hydrocortisone 500 mg or more
  • ECMO

About University Medical Centre Maribor

University Medical Centre Maribor is a leading healthcare institution in Slovenia, dedicated to advancing medical research and improving patient care through innovative clinical trials. As a prominent academic center, it integrates cutting-edge research with clinical practice, fostering collaboration among healthcare professionals, researchers, and patients. The institution is committed to enhancing medical knowledge and treatment options across various specialties, ensuring adherence to the highest ethical standards and regulatory compliance. With a focus on patient safety and well-being, University Medical Centre Maribor plays a pivotal role in contributing to the global medical community through its rigorous clinical research initiatives.

Locations

Maribor, , Slovenia

Maribor, , Slovenia

Patients applied

0 patients applied

Trial Officials

Andreja Möller Petrun, PhD

Study Chair

University Medical Centre Maribor

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported