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Recruiting Not applicable

Low Serum Creatinine as a Predictor of Prolonged Mechanical Ventilation and Weaning Failure

NCT07177183 · tracked via the Priya Life Science Czechia tracker
Phase
Not applicable
Started
2026-02-02
Last updated
2026-02-05

Condition(s) studied

Prolonged Mechanical VentilationCritical Illness

Investigational drug(s) / intervention(s)

Dietary supplement creatineDietary supplement - placeboNo intervention

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients \<18 years of age * Patients admitted to post-ICU care units at Chronicare Group a.s. in the Czech Republic within 12 months Exclusion Criteria: * Patients who are unlikely to be weaned from ventilatory support. * Patients in palliative care or with a survival probability of \<3 months * Patients with advanced malignancy * Patients with a history of chronic kidney disease * Patients with a history of chronic liver disease * Patients with supranormal serum creatinine on admission to the post-ICU care unit * Patients who refused to sign the Informed Consent with participation in the study.

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)

FacilityCityRegionStatus
Chronicare Mund s.r.o. Brno Czechia Recruiting
Chronicare s.r.o. Milovice Czechia Recruiting
Official registry record

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