Skip to content

Norepinephrine administration timing

Time to norepinephrine in sepsis – a prospective inception cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN13420347
Enrollment
61
Registered
2026-02-03
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Sepsis with hypotension Infections and Infestations

Interventions

This is an observational study. Participants are identified at the Emergency Department (ED) based on clinical criteria (suspected sepsis and hypotension). Data is collected prospectively using a pape
the study only monitors and records the timing of interventions and fluid volumes as they occur in real-time or as documented in the medical records during the first 24 hours of care. Study design an

Sponsors

Region Stockholm
Lead Sponsor
Karolinska Institutet
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years 2. Suspected sepsis defined as, blood cultures obtained and intravenous antibiotics administered. 3. Hypotension defined as MAP < 65 mmHg. 4. eSOFA 2 points or more

Exclusion criteria

Exclusion criteria: Prior enrollment in this study.

Countries

Sweden

Contacts

Public ContactMikael Hallengren
mikael.hallengren@regionstockholm.se+460812355000

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: May 7, 2026