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NCT04726514 · ClinicalTrials.gov registry record · NA

SleepFlexTM Treatment of Obstructive Sleep Apnea

A NA study of Obstructive Sleep Apnea, sponsored by Berendo Scientific.

Completed
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT04726514: Completed NA study of Obstructive Sleep Apnea, sponsored by Berendo Scientific.

NCT04726514 is a NA study of Obstructive Sleep Apnea that has completed, run by Berendo Scientific. The registered enrollment target is 10 participants, below the 222-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04726514, a NA study of Obstructive Sleep Apnea, has completed, sponsored by Berendo Scientific.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the safety and effectiveness of the SleepFlex program for treatment of mild to moderate OSA

Primary Outcome

Number of participants with absence of serious adverse events related to the SleepFlex system.

Conditions Studied

Interventions

  • DEVICE SleepFlex

Study Locations (1)

California

  • Tower Sleep Medicine - Los Angeles

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2021-07-20
Est. Completion 2022-05-31
Phase NA
Berendo Scientific

1 total trials

What the finished NCT04726514 record still lists

NCT04726514 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 222-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Obstructive Sleep Apnea appearing as the primary indexed condition, and to 1 intervention - of which SleepFlex is the first listed.

NCT04726514 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT04726514 about?

NCT04726514 is a clinical study titled "SleepFlexTM Treatment of Obstructive Sleep Apnea". The purpose of this study is to evaluate the safety and effectiveness of the SleepFlex program for treatment of mild to moderate OSA

What is the current status of trial NCT04726514?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2021-07-20. Estimated completion is 2022-05-31.

What conditions does trial NCT04726514 study?

This clinical trial studies the following conditions: Obstructive Sleep Apnea.

What interventions are being tested in trial NCT04726514?

The interventions under investigation include: SleepFlex (DEVICE).

Who is sponsoring clinical trial NCT04726514?

This trial is sponsored by Berendo Scientific, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04726514 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obstructive Sleep Apnea

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04726514's enrollment target sits among peer trials

10 152nd of 155 higher than 2 of 155 other Obstructive Sleep Apnea trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obstructive Sleep Apnea 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 NCT04726514, the US trial registry maintained by the National Library of Medicine. NCT04726514 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.