About this trial
The hypothesis is that a daily supplement of 22 mg of zinc over 12 months can reduce in-flammatory biomarkers in acutely hospitalized older adults aged ≥ 65 years.
The aims are to determine, in acutely hospitalized older adults aged ≥ 65 years, if a daily supplement of 22 mg of zinc over 12 months compared to control can decrease inflammato-ry biomarkers, reduce symptoms of self-reported infection, reduce readmission and mortali-ty, increase QoL, increase physical performance, investigate potential adverse events to zinc supplement, and the changes in inflammatory biomarkers. It will also be studied if albumin-corrected zinc in plasma is a more accurate method for assessing zinc status than ordinary plasma zinc.
Eligibility criteria
Qualifiers
above 65 years old included in ZOOM out ( clinical trials no: NCT07367412)
admittet at the medical emergency department Herlev Hospital
Disqualifiers
Patients receiving zinc supplements (>10 mg daily) at time of inclusion
Patients with terminal illness (life expectancy < 6 months, estimated by Clinical Frailty Scale ≥8)
Patients receiving parenteral nutrition (partial or complete)
Patients treated with hemodialysis or peritoneal dialysis
Trial design
Treatments tested in this trial
- Zinc Supplement