Assistance Publique - Hôpitaux de Marseille
Marseille, 13005, France
NCT Number: NCT07052084
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 3
Marseille, 13005, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Low dose of vasopressin (0.02ui /min), maximum 5 days
NaCl 0.9 %, maximum 5 days
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)
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)
Time frame: 28 days after administration of experimental drug (D28)
Time frame: Between administration of experimental drug (H0), 24 hours after (H24), and 48 hours after (H48)
Time frame: 5 days after administration of experimental drug (D5)
Maximum dose
Time frame: 28 days after administration of experimental drug (D28)
Number of days alive without renal replacement therapy
Time frame: 28 days after administration of experimental drug (D28)
Number of days alive without mechanical ventilation
Time frame: 28 days after administration of experimental drug (D28)
Time frame: 28 days after administration of experimental drug (D28)
Time frame: 28 days after administration of experimental drug (D28)
Time frame: 28 days after administration of experimental drug (D28)
Time frame: 28 days after administration of experimental drug (D28)
Time frame: 28 days after administration of experimental drug (D28)
Contact information is provided by the study sponsor or research team.
Assistance Publique Hopitaux De Marseille
Other
Systematic Adjunction of Vasopressine in Hyperkinetic Septic Shock Patients - A Multicentric RCT
Acronym: SAVSepticShock
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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