NCT06238362

TheraPAP Equivalence Crossover Study

Randomized Crossover Study to Compare Effectiveness of a Device Providing Pressure Drops During Inspiration (TPAP) to Continuous Positive Airway Pressure (CPAP) in Obstructive Sleep Apnea (OSA)
SleepRes Inc.·ClinicalTrials.gov·otherRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Obstructive Sleep Apnea
Drug/Device/Intervention
TPAP
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
SleepRes Inc.
Location
Clarksville, United States of America
Timeline & enrollment
Phase
N/A
Start date
Mar 07, 2024
End date
Jul 30, 2024
Enrollment
150 participants
Primary outcome

Apnea/Hypopnea Index

Summary

The present study, TheraEquivalence, is a Phase 2 crossover study designed to examine the
 efficacy and safety of TheraPAP (TPAP) vs. CPAP alone in the treatment of OSA.

ICD-10 classifications
Sleep apnoeaSleep disordersSleep disorder, unspecifiedPrimary sleep apnoea of newbornNonorganic sleep disorders
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06238362
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06238362 through Pure Global AI's free database. This phase not specified trial is sponsored by SleepRes Inc. and is currently Recruiting. The study focuses on Obstructive Sleep Apnea. Target enrollment is 150 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.