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Weaning Approaches for Vasopressin in Sepsis
Plain-language guide to NCT07067866: phase 3 randomized trial of Vasopressin, 82 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT07067866
- Phase
- phase 3
- Status
- recruiting participants
- Start
- 2025-10-01
- Completion (planned or actual)
- 2027-12-31
- Participants
- 82 (estimated)
- Design
- randomized, open label (everyone knows who gets what), treatment
- Conditions studied
- Septic Shock
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
In this phase 3 trial, researchers set out to test Vasopressin.
It had two arms (groups): Titrated group (experimental) and Abrupt group (active comparator).
The registry classes the interventions as other.
More on the Plan
Catecholamine infusions are usually tapered gradually in a titrated manner.
However, little is known about how to manage adjunctive therapies such as vasopressin.
While catecholamines have a short half-life (2-3 minutes), vasopressin's half-life ranges from 10 to 20 minutes.
Although endogenous vasopressin levels are depleted in the early phase of shock, they are restored during recovery.
Who Took Part
The registry lists 82 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: Age over 18 years. Admitted to the Intensive Care Unit. Patients with vasopressor dependent sepsis. Receiving combined norepinephrine and vasopressin therapy.
The full record lists 4 inclusion and 2 exclusion criteria.
How the Study Was Run
The set-up was randomized, parallel-group and open-label.
The participants were allocated by chance, so the Vasopressin group and the comparison group should start out alike.
The Vasopressin group and the comparison group ran side by side rather than switching.
Everyone knew when Vasopressin was being given (open label), which is simpler to run but leaves more room for expectations to affect what is reported.
It started in 2025-10-01 with completion listed for 2027-12-31.
It ran at 1 site in Brazil.
Its stated primary purpose is treatment.
What Was Measured
The main thing measured (primary outcome): Hypotension within the first 24 hours (time frame: 24 hours).
It also tracked 9 secondary outcomes, for example Hypotension stratified according to vasopressin duration, Hypotension within the first hour, Vasopressor-free days, Vasopressin-free days, Renal replacement therapy and Cardiac arrhythmias.
What This Means in Plain Language
Put simply, this is a phase 3, randomized trial of Vasopressin in 82 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.