Health Condition 1: O- Medical and Surgical Health Condition 2: C00-D49- Neoplasms
Conditions
Interventions
Intervention1: Nil: NA
Control Intervention1: Nil: NA
Sponsors
Amsterdam University Medical Centers, location â??AMCâ??
Eligibility
Inclusion criteria
Inclusion criteria: 1. admitted to a participating ICU 2. receiving invasive ventilation within 3 days of ICU admission and 3. duration of ventilation more than 24 hours
Exclusion criteria
Exclusion criteria: 1. Age less than 18 years 2. patients transferred under invasive ventilation from another ICU
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is a composite of various aspects of fluid therapy, including total volumes of types of fluids administered in the first three days after start of invasive ventilation and total volume of fluids infused in the first seven days after start of invasive ventilation.Timepoint: At day 3 and day 7 of start of invasive ventilation in ICU | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include timing of start, type, and duration of continuous administration of vasopressors; timing of start, infusion time and types of administered diuretics; daily urine output and cumulative fluid balances; and typical ICU outcomes, like duration of ventilation, lengths of stay in ICU and hospital, and mortality in the ICU and hospital.Timepoint: At day 28, 60 and 90 | — |
Countries
India, Netherlands
Contacts
Public ContactDr Sheila Nainan Myatra
Tata Memorial Hospital
Outcome results
None listed