Current partner codePEPTIDESDE
NCT07052084·Phase 3·INTERVENTIONAL

Systematic Adjunction of Vasopressine in Septic Shock

Status

Not yet recruiting

Phase

Phase 3

Enrollment

120

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Septic shock is a syndrome associated with severe infection and a mortality rate of approximately 45%. In line with current recommendations, norepinephrine is the first-line vasopressor used in patients with septic shock. In a previous study, norepinephrine doses above 1 µg/kg/min were associated with mortality rates over 90%. In the same study, doses above 0.3 µg/kg/min were associated with a mortality rate of 40%. An increased mortality compared to the general 40% mortality of septic shock appears to be associated with norepinephrine doses as low as 0.3 µg/kg/min. Vasopressin stimulates V1 receptors, primarily located on vascular smooth muscle cells. When V1a receptors are stimulated, they induce vasoconstriction by activating protein kinase C via a Gq protein and various second messengers. Its use is validated in refractory shock states by international guidelines as a second-line vasopressor. This indication was further reinforced in the 2021 update of the septic shock management recommendations. The VASST study, a randomized controlled trial, assessed the effects of vasopressin versus norepinephrine in septic shock. It found no overall difference in mortality between the two groups. However, in less severe cases where norepinephrine doses were below 14 µg/min before randomization, vasopressin was associated with significantly lower mortality, suggesting potential benefits from early introduction of a second vasopressor. The VANISH trial failed to confirm this hypothesis, possibly due to broad inclusion criteria and unclear protocol regarding the combined use of both agents. Our hypothesis is that (1) vasopressin is beneficial when used synergistically with norepinephrine; (2) due to its negative effect on cardiac output (as shown in previous studies), vasopressin should only be administered to patients in the hyperdynamic phase of septic shock. The hypothesis is that the systematic addition of vasopressin to norepinephrine therapy in a hyperdynamic septic shock subpopulation would improve patient outcomes.

Interventions

Treatment arms and agents.

DRUG

Vasopressin administration

Low dose of vasopressin (0.02ui /min), maximum 5 days

DRUG

Sodium chloride administration

NaCl 0.9 %, maximum 5 days

Timeline

From registration to results.

  1. First posted

    Jul 4, 2025

  2. Study start

    Jan 2026

  3. Primary completion

    Feb 2028

  4. Study completion

    Feb 2028

  5. Results posted

    Not reported

  6. Registry updated

    Aug 8, 2025

Outcomes

What the study measures.

Primary outcomes

SOFA score comparison between the two groups

Time frame · 48 hours after administration of experimental drug (H48)

Sepsis-related Organ Failure Assessment, 0 to 24 points (higher scores indicate more severe organ dysfunction)

Secondary outcomes

SOFA score comparison between the two groups

Time frame · 120 hours after administration of experimental drug (H120)

Sepsis-related Organ Failure Assessment, 0 to 24 points (higher scores indicate more severe organ dysfunction)

Mortality comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Lactatemia decrease comparison between the two groups

Time frame · Between administration of experimental drug (H0), 24 hours after (H24), and 48 hours after (H48)

Noradrenaline use comparison between the two groups

Time frame · 5 days after administration of experimental drug (D5)

Maximum dose

Renal function comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Number of days alive without renal replacement therapy

Respiratory function comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Number of days alive without mechanical ventilation

Occurrence of myocardial ischemia comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Occurrence of cardiogenic shock comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Occurrence of mesenteric ischemia comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Occurrence of digital ischemia comparison between the two groups

Time frame · 28 days after administration of experimental drug (D28)

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Patient aged 18 or over * Patient who has consented to take part in the research or patient whose close relative has consented to take part in the research or, failing that, patient being included in an emergency situation * Patient in septic shock with adapted cardiac output * Patient in whom noradrenaline dosage has been greater than 0.3μg/kg/min for less than 12 hours * Patients benefiting from or affiliated to social security Exclusion Criteria: * Patient with acute coronary syndrome * Patient with known history of acute coronary syndrome * Patient with suspected mesenteric ischemia * Patient with hyponatremia \< 130mmol/L, * Known allergy to vasopressin or its excipients * Minors * Pregnant women * Patients under legal guardianship or curatorship * Patients under judicial protection.

Study locations

1 registered sites.

France. Showing up to 24 locations stored in the fast local snapshot.

Assistance Publique - Hôpitaux de Marseille

Marseille, France

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Vasopressin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.