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NCT06413134 · ClinicalTrials.gov registry record · NA

KPAP Adherence Crossover Study

A NA study, sponsored by SleepRes.

Not yet
Registry status
NA
Development phase
30
Enrollment target

NCT06413134: Clinical Trial NA study, sponsored by SleepRes.

NCT06413134 is a NA study that has not yet begun recruiting, run by SleepRes. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06413134, a NA study, has not yet begun recruiting, sponsored by SleepRes.

NOT YET RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

A device able to provide less positive airway pressure (PAP) for the entire duration of inspiration and roughly half the duration of expiration, designated KPAP, is being developed by SleepRes for the treatment of obstructive sleep apnea (OSA). In prior studies, the administration of higher inspiratory than expiratory PAP did not substantially increase treatment efficacy or adherence to continuous PAP (CPAP), which remains low. In our recent investigation, we demonstrated that the addition of a resistor to the CPAP circuit to reduce inspiratory PAP increased subjective comfort. In another study, we showed that KPAP improved subjective comfort during wakefulness vs. fixed CPAP, while maintaining treatment efficacy. The present study, KPAP Adherence 1, is a randomized, crossover study designed to examine whether KPAP can improve adherence over APAP as an at home treatment for OSA.

Primary Outcome

Number of hours for which therapy is used per night

Interventions

  • DEVICE KPAP
  • DEVICE APAP

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2026-07-01
Est. Completion 2026-12-31
Phase NA
SleepRes

3 total trials

What is known before NCT06413134 opens enrollment

NCT06413134 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT06413134 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06413134 about?

NCT06413134 is a clinical study titled "KPAP Adherence Crossover Study". A device able to provide less positive airway pressure (PAP) for the entire duration of inspiration and roughly half the duration of expiration, designated KPAP, is being developed by SleepRes for the treatment of obstructive sleep apnea (OSA). In prior studies, the administration of higher inspirat...

What is the current status of trial NCT06413134?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2026-07-01. Estimated completion is 2026-12-31.

What interventions are being tested in trial NCT06413134?

The interventions under investigation include: KPAP (DEVICE), APAP (DEVICE).

Who is sponsoring clinical trial NCT06413134?

This trial is sponsored by SleepRes, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06413134's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 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 NCT06413134, the US trial registry maintained by the National Library of Medicine. NCT06413134 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.