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NCT02130388 · ClinicalTrials.gov registry record · NA

The Impact of Zinc Supplementation on Innate Immunity and Patient Safety in Sepsis

A NA study, sponsored by Ohio State University.

Terminated
Registry status
NA
Development phase
10
Enrollment target

NCT02130388: Clinical Trial NA study, sponsored by Ohio State University.

NCT02130388 is a NA study that was terminated before completion, run by Ohio State University. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02130388, a NA study, was terminated before completion, sponsored by Ohio State University.

TERMINATED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

Sepsis is the body's response to a life-threatening infection. This study will determine if zinc supplementation is safe to use in patients with severe sepsis or septic shock. This study will also gather preliminary information to evaluate the impact that zinc has on the immune system (the body's defense system against infection) and whether zinc can help monocytes and macrophages (specific types of cells that remove infections from the body) work more effectively.

Primary Outcome

This study consists of receiving a dose of zinc once daily while in the ICU for up to 7 days, up to four timed blood draws over the first 10 days of your hospitalization (if you remain in the hospital that long), and collecting some immune cells from your blood +/- lungs. We will review your medical chart at the time of the blood draws and again when you are getting ready for discharge.

Interventions

  • DIETARY_SUPPLEMENT Zinc

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2014-05
Est. Completion 2019-03
Phase NA
Ohio State University

552 total trials

Why NCT02130388 stopped before completion

NCT02130388 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Zinc is the first listed.

NCT02130388 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02130388 about?

NCT02130388 is a clinical study titled "The Impact of Zinc Supplementation on Innate Immunity and Patient Safety in Sepsis". Sepsis is the body's response to a life-threatening infection. This study will determine if zinc supplementation is safe to use in patients with severe sepsis or septic shock. This study will also gather preliminary information to evaluate the impact that zinc has on the immune system (the body's de...

What is the current status of trial NCT02130388?

This trial is currently terminated. It is a NA study. The enrollment target is 10 participants. The study started on 2014-05. Estimated completion is 2019-03.

What interventions are being tested in trial NCT02130388?

The interventions under investigation include: Zinc (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02130388?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02130388's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02130388, the US trial registry maintained by the National Library of Medicine. NCT02130388 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.