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NCT02202811 · ClinicalTrials.gov registry record · NA

Circadian Rhythms and Cardiovascular Risk

A NA study, sponsored by Oregon Health and Science University.

Completed
Registry status
NA
Development phase
39
Enrollment target

NCT02202811: Completed NA study, sponsored by Oregon Health and Science University.

NCT02202811 is a NA study that has completed, run by Oregon Health and Science University. The registered enrollment target is 39 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02202811, a NA study, has completed, sponsored by Oregon Health and Science University.

COMPLETED
Registry status
NA
Development phase
39 participants
Enrollment target

Study Summary

The purpose of this study is to understand how behaviors and the effects of the body's internal clock (called the circadian pacemaker) affect the control of the heart and blood pressure. People with Obstructive Sleep Apnea (OSA) are hypothesized to have altered circadian amplitudes in certain key indices of cardiovascular (CV) and an abnormally advanced circadian phase in some of the same key indices of CV risk. The investigators hypothesize that such changes, taken together, may explain the different timing of heart attack and sudden cardiac death in OSA.

Primary Outcome

Comparisons will be made between participants with obstructive sleep apnea (OSA) and healthy controls of the circadian amplitude of plasma epinephrine concentration during resting baseline conditions. Circadian rhythm amplitude will be assessed by cosinor analysis of all resting measurements obtained throughout the protocol assessed under constant conditions but at varied circadian phases.

Interventions

  • BEHAVIORAL Forced Desynchrony

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2014-08
Est. Completion 2020-03-09
Phase NA

What the finished NCT02202811 record still lists

NCT02202811 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

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

NCT02202811 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02202811 about?

NCT02202811 is a clinical study titled "Circadian Rhythms and Cardiovascular Risk". The purpose of this study is to understand how behaviors and the effects of the body's internal clock (called the circadian pacemaker) affect the control of the heart and blood pressure. People with Obstructive Sleep Apnea (OSA) are hypothesized to have altered circadian amplitudes in certain key i...

What is the current status of trial NCT02202811?

This trial is currently completed. It is a NA study. The enrollment target is 39 participants. The study started on 2014-08. Estimated completion is 2020-03-09.

What interventions are being tested in trial NCT02202811?

The interventions under investigation include: Forced Desynchrony (BEHAVIORAL).

Who is sponsoring clinical trial NCT02202811?

This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02202811's enrollment target sits among peer trials

39 1536th of 2000 higher than 463 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 NCT02202811, the US trial registry maintained by the National Library of Medicine. NCT02202811 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.