Low Serum Creatinine as a Predictor of Prolonged Mechanical Ventilation and Weaning Failure
Condition(s) studied
Investigational drug(s) / intervention(s)
Dietary supplement creatine: Dietary supplement creatine. The dosage of creatine will be as follows: for the first 7 days after enrolment, the daily dose will be 2x5g. From days 8 to 21, the daily dose will be 1x5g. The substance will be administered orally or through a nasogastric tube.
Dietary supplement - placebo: Dietary supplement polydextrose as a placebo. The dosage of placebo will be as follows: for the first 7 days after enrolment, the daily dose will be 2x5g. From days 8 to 21, the daily dose will be 1x5g. The substance will be administered orally or through a nasogastric tube.
No intervention: Patients in Group 1 will serve as controls and will receive no intervention, only standard care.
Study summary
The main objective of the study is to determine whether a subnormal serum creatinine value upon admission to the Post-ICU Care Unit predicts the need for prolonged ventilatory support. A parallel objective of the study is to determine whether exogenous in-take of the dietary supplement creatine in patients with subnormal serum creatinine value is associated with a shortened duration of ventilatory support and improved patients outcome.
Eligibility
Primary outcome measure(s)
- Ventilator-free hours — 21 days
The primary endpoint of the study will be the "ventilator-free hours", i.e. the total number of hours that the patient was without ventilator support
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Chronicare Mund s.r.o. | Brno | Czechia | Recruiting |
| Chronicare s.r.o. | Milovice | Czechia | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07177183 on ClinicalTrials.gov ↗ ← All trials in Czechia