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NCT02770092 · ClinicalTrials.gov registry record · NA

CHF COPD Sip Feed Anabolic Response

A NA study, sponsored by Texas A&M University.

Completed
Registry status
NA
Development phase
90
Enrollment target

NCT02770092: Completed NA study, sponsored by Texas A&M University.

NCT02770092 is a NA study that has completed, run by Texas A&M University. The registered enrollment target is 90 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02770092, a NA study, has completed, sponsored by Texas A&M University.

COMPLETED
Registry status
NA
Development phase
90 participants
Enrollment target

Study Summary

Weight loss commonly occurs in patients with chronic heart failure (CHF) and chronic obstructive pulmonary disorder (COPD), negatively influencing their quality of life, treatment response and survival. Loss of muscle protein is generally a central component of weight loss in CHF and COPD patients, but patients also have reductions in fat mass and bone density, independent of the severity of the disease state. The purpose of this study is to provide detailed insight in disease related gut function by obtaining information on gut permeability, digestion and absorption of glucose, fat and protein in CHF and COPD patients compared to matched healthy controls. This will provide required information that is necessary to implement new strategies to develop optimal nutritional regimen in CHF and COPD.

Primary Outcome

Change in whole-body protein synthesis rate after intake of meal

Interventions

  • OTHER sip feeding with stable isotope infusion

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2016-02-10
Est. Completion 2018-05-15
Phase NA
Texas A&M University

95 total trials

What the finished NCT02770092 record still lists

NCT02770092 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which sip feeding with stable isotope infusion is the first listed.

NCT02770092 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02770092 about?

NCT02770092 is a clinical study titled "CHF COPD Sip Feed Anabolic Response". Weight loss commonly occurs in patients with chronic heart failure (CHF) and chronic obstructive pulmonary disorder (COPD), negatively influencing their quality of life, treatment response and survival. Loss of muscle protein is generally a central component of weight loss in CHF and COPD patients, ...

What is the current status of trial NCT02770092?

This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2016-02-10. Estimated completion is 2018-05-15.

What interventions are being tested in trial NCT02770092?

The interventions under investigation include: sip feeding with stable isotope infusion (OTHER).

Who is sponsoring clinical trial NCT02770092?

This trial is sponsored by Texas A&M University, which has 95 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02770092's enrollment target sits among peer trials

90 941st of 2000 higher than 1,029 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 NCT02770092, the US trial registry maintained by the National Library of Medicine. NCT02770092 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.