Zinc Supplementation and Inflammation in Older Medical Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorHerlev Hospital

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

Treatment groups

220 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators