A prospective randomized controlled trial to investigate the effect of early administration of antibiotics for patients with suspected sepsis

A prospective randomized controlled trial to investigate the effect of early administration of antibiotics for patients with suspected sepsis - PHANTASi trial- PreHospital ANTibiotics against Sepsis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON43665

Enrollment

2800

Registered

2014-03-27

Start date

2014-06-30

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

bloodpoisoning sepsis

Interventions

the prehospital treatment group will receive 2000 mg ceftriaxone intravenously. After samples of bloodcultures are taken. The control group will receive no intervention

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) in the history signs of an infection and a body temperature of > 38 degrees celcius or 20/min; A heart rate of > 90/min ;

Exclusion criteria

Exclusion criteria: - age

Design outcomes

Primary

Measure	Time frame
reduction of mortality in patients with sepsis	—

Secondary

Measure	Time frame
- Length of hospital stay , Length of ICU stay if applicable - Door to needle time in control group - Adverse events in the intervention group and the control group - Quality of life after one month after discharge from the hospital -- Number of blood cultures with Bacteria resistant to ceftriaxone - Hour of transfer to the intensive care, medium care or to a normal ward	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)