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VAsopressin LOading for Refractory septic shock VALOR study

VAsopressin LOading for Refractory septic shock VALOR study - VALOR study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000044041
Enrollment
100
Registered
2021-04-26
Start date
2021-04-26
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

septic shock

Interventions

None listed

Sponsors

Hitachi General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.age>=18 2.septic shock (Sepsis-3) 3.require vasopressin administration in the patients given continuous noradrenaline>=0.2gamma 4.not given continuous steroid therapy 5.arterial line inserted 6.informed consent

Exclusion criteria

Exclusion criteria: End of life/Terminal care

Design outcomes

Primary

MeasureTime frame
The catecholamine index change six hours after the initiation of continuous vasopressin administration

Countries

Japan

Contacts

Public ContactKensuke Nakamura

Hitachi General Hospital Emergency and Critical Care Medicine

mamashockpapashock@yahoo.co.jp0294-23-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026