NCT07744854

Brief Summary

The existing PranaQ system utilizes a fingertip sensor that captures PPG(Photoplethysmography) and accelerometer data, and its clinical validation is well-established. While PPG alone has shown effectiveness in diagnosing obstructive sleep apnea, its limited data channels restrict comprehensive evaluation. For instance, it struggles to link apnea events with body position or differentiate between central and obstructive sleep apnea. To address these limitations, the PranaQ system incorporates new sensors, specifically the chest patch sensor, to monitor respiratory movements via accelerometer signals. The additional respiration signal has the potential to improve diagnostic accuracy for apnea through additional information from respiratory effort.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P50-P75 for all trials

Timeline
8mo left

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress21%
Jun 2026Mar 2027

Study Start

First participant enrolled

June 5, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 29, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 4, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 23, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 23, 2027

Last Updated

August 4, 2026

Status Verified

July 1, 2026

Enrollment Period

10 months

First QC Date

July 29, 2026

Last Update Submit

July 29, 2026

Conditions

Keywords

apneachest patch

Outcome Measures

Primary Outcomes (3)

  • Respiratory Rate

    PSG recording estimated respiratory rate as ground truth to compare with the C-TraQ-generated respiratory rate.

    one night

  • Sleep Position

    Sleep Position measured by PSG as ground truth to compare with C-TraQ generated sleep position

    One night

  • AHI

    Technician labeled AHI based on PSG signal to compare with PranaQ system's prediction.

    One night

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patient who is scheduled for a sleep study.

You may qualify if:

  • Subjects must be 18 years of age or older.

You may not qualify if:

  • Opioids use
  • Chronic Obstructive Lung Disease, Global Initiative for Chronic Obstructive
  • Lung Disease (GOLD) categorization 3 or 4
  • Devastating strokes, with a modified Rankin score (mRS) ≥ 4
  • Interstitial lung disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Veterans General Hospital

Taipei, Taiwan, 201, Taiwan

RECRUITING

MeSH Terms

Conditions

Sleep Apnea SyndromesSleep Apnea, CentralApnea

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Ke Wei Chen, M.D.

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 29, 2026

First Posted

August 4, 2026

Study Start

June 5, 2026

Primary Completion (Estimated)

March 23, 2027

Study Completion (Estimated)

March 23, 2027

Last Updated

August 4, 2026

Record last verified: 2026-07

Locations