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NCT Number: NCT07052084

Systematic Adjunction of Vasopressine in Septic Shock

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Assistance Publique - Hôpitaux de Marseille

Marseille, 13005, France

Location contact

Gary Duclos, MD

CONTACT

[email protected]

04 91 96 55 31 ext. +33

Gary Duclos, MD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Vasopressin administration

Drug

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

Sodium chloride administration

Drug

NaCl 0.9 %, maximum 5 days

Primary outcomes

  1. 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

  1. 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)

  2. Mortality comparison between the two groups

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

  3. Lactatemia decrease comparison between the two groups

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

  4. Noradrenaline use comparison between the two groups

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

    Maximum dose

  5. 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

  6. Respiratory function comparison between the two groups

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

    Number of days alive without mechanical ventilation

  7. Occurrence of myocardial ischemia comparison between the two groups

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

  8. Occurrence of cardiogenic shock comparison between the two groups

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

  9. Occurrence of mesenteric ischemia comparison between the two groups

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

  10. Occurrence of digital ischemia comparison between the two groups

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

  11. Occurrence of atrial fibrillation comparison between the two groups

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

  12. Occurrence of a thromboembolic event comparison between the two groups

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

Study contacts

Contact information is provided by the study sponsor or research team.

Gary Duclos, MD

CONTACT

[email protected]

04 91 96 55 31 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique Hopitaux De Marseille

Other

Registry information

Official study title

Systematic Adjunction of Vasopressine in Hyperkinetic Septic Shock Patients - A Multicentric RCT

Acronym: SAVSepticShock

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jul 4, 2025
Registry last updated
Aug 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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