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NCT02293616 · ClinicalTrials.gov registry record · NA

Strength Testing After Nitrate Delivery (STAND) in ICU Patients

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
25
Enrollment target

NCT02293616 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 25 participants.

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The verdict

NCT02293616, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target

Study Summary

It is well documented that intensive care unit (ICU) patients have lower levels of skeletal muscle strength compared to non-ICU patients upon hospital discharge, and this weakness affects the patient's ability to perform basic activities of daily living upon hospital discharge and for extended periods thereafter. Recently, critically ill ICU patients have been shown to have lower nitric oxide levels. These patients often suffer from a disturbed homeostasis with circulatory and metabolic abnormalities that may potentially contribute to their ICU acquired weakness. Given the recent research showing dietary nitrate supplementation can increase nitric oxide levels and improve exercise tolerance in healthy and diseased older individuals, our aim is to investigate the importance of nitrate supplementation in ICU patients with focus on physical function and ICU acquired muscle weakness.

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT Nitrate Rich Beetroot Juice

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2015-06
Est. Completion 2017-04
Phase NA

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT02293616

The ClinicalTrials.gov registry entry for NCT02293616 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02293616 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02293616 about?

NCT02293616 is a clinical study titled "Strength Testing After Nitrate Delivery (STAND) in ICU Patients". It is well documented that intensive care unit (ICU) patients have lower levels of skeletal muscle strength compared to non-ICU patients upon hospital discharge, and this weakness affects the patient's ability to perform basic activities of daily living upon hospital discharge and for extended perio...

What is the current status of trial NCT02293616?

This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2015-06. Estimated completion is 2017-04.

What interventions are being tested in trial NCT02293616?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Nitrate Rich Beetroot Juice (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02293616?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.