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Use of Vasopressin in Patients at High Risk of Acute Kidney Injury Admitted to the ICU
Plain-language guide to NCT06547892: phase 2 randomized trial of Vasopressin, 60 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT06547892
- Phase
- phase 2
- Status
- recruiting participants
- Start
- 2025-04-10
- Completion (planned or actual)
- 2025-10-10
- Participants
- 60 (estimated)
- Design
- randomized, quadruple-blind, prevention
- Conditions studied
- Critical Illness
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
In this phase 2 trial, researchers set out to test Vasopressin.
It had two arms (groups): Vasopressin (experimental) and Placebo (placebo comparator).
The registry classes the interventions as drug and other.
More on the Plan
This is a multicenter, placebo-controlled, double-blind, randomized feasibility clinical trial with a proposal to include 60 patients across 3 to 4 research centers.
The primary objective is to evaluate the feasibility of the study, specifically adherence to the established protocol and the monitoring of potential adverse effects during its conduct.
Who Took Part
The registry lists 60 planned participants were the target.
It was open to people of any sex aged from 18 years with no upper age limit.
Healthy volunteers were not accepted; participants needed the condition being studied.
Examples of who could join: Adult patients (≥18 years old);. Admitted to intensive care units;.
The full record lists 3 inclusion and 12 exclusion criteria; among the exclusions: time since admission to the icu greater than 24 hours;; use of vasopressors at the time of inclusion;; MAP \>90 mmHg;.
How the Study Was Run
Design: randomized, parallel-group and quadruple-blind.
Because people in this Vasopressin study were split into groups at random, differences between the groups are less likely to reflect who happened to join each one.
The Vasopressin group and the comparison group ran side by side rather than switching.
Blinding on both sides kept the participants and researchers unaware of who received Vasopressin.
Those kept unaware of assignments: participant, care provider, investigator and outcomes assessor.
It started in 2025-04-10 with completion listed for 2025-10-10.
It ran at 1 site in Brazil.
Its stated primary purpose is prevention.
What Was Measured
Researchers chose this as the main measure: Feasibility (time frame: 6 months).
It also tracked 1 secondary outcome, for example Creatinine, in mg/dL.
What This Means in Plain Language
Put simply, this is a phase 2, randomized trial of Vasopressin in 60 people.
It is still recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Vasopressin compound page, all human trials.
Our Notes on the Compound
Vasopressin: A 9-amino-acid hormone (antidiuretic hormone) that controls water balance and blood vessel tone; used in septic shock.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.