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Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

3 clinical studies listed.

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Vasodilatory Shock

Tundra lists 3 Vasodilatory Shock clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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ACTIVE NOT RECRUITING

NCT07568275

Comparison of Angiotensin II to Standard Dose Vasopressors on Change in Arterial Elastance

A study to see whether a medication called Angiotensin II works better than the routinely used medication to raise blood pressure in people with liver disease who are experiencing a serious drop in blood pressure. The investigators want to find out if Angiotensin II can help the heart and blood vessels work together more effectively than standard treatments.

Gender: All

Ages: 18 Years - Any

Updated: 2026-05-05

1 state

Septic Shock
Cirrhosis
Vasodilatory Shock
+1
ENROLLING BY INVITATION

NCT07212686

Synthetic Angiotensin II/Giapreza in Pediatric Patients With Refractory Hypotension

The goal of this clinical trial is to determine the safety and efficacy of Angiotensin-II in the treatment of pediatric patients in fluid refractory vasodilatory shock. The main questions it aims to answer are: * To evaluate the change in blood pressure or reduction of vasoactive requirements (norepinephrine equivalent dosing) after initiating Angiotensin II * To establish the safety and tolerability of Angiotensin-II in pediatric patients Participants will receive Angiotensin-II in addition to standard of care therapy for vasodilatory shock. * The study team will then monitor the patient's vital signs, blood work, and for any potential side effects from the drug. * An ultrasound will be performed to look at blood flow through the kidney in the setting of vasodilatory shock. * A follow up phone call to check in with the patient will be performed 28 days after enrollment.

Gender: All

Ages: 0 Days - 18 Years

Updated: 2025-10-08

1 state

Vasodilatory Shock
RECRUITING

NCT06351150

Efficacy and Safety of Angiotensin II Injection Versus Placebo in Patients With Refractory Distributed Shock

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.

Gender: All

Ages: 18 Years - Any

Updated: 2025-01-23

24 states

Vasodilatory Shock