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ThermoSmart® Versus Conventional Humidification in Continuous Positive Airway Pressure (CPAP)

This study is currently recruiting participants.
Verified by Fisher and Paykel Healthcare, September 2008

Sponsors and Collaborators: Fisher and Paykel Healthcare
Suburban Lung Associates
Information provided by: Fisher and Paykel Healthcare
ClinicalTrials.gov Identifier: NCT00751335
  Purpose

That ThermoSMart humidification will result in greater compliance (mask on time, objective and subjective sleep quality than conventional humidification.


Condition Intervention
Sleep Apnea, Obstructive
Device: Heated breathing tube (CPAP with ThermoSmart)
Device: Non heated breathing tube (CPAP with conventional humidification)

MedlinePlus related topics:   Sleep Apnea   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double Blind (Subject, Investigator), Crossover Assignment, Efficacy Study
Official Title:   Prospective, Randomized, Double-Blind Cross-Over Study Comparing ThermoSmart® to Conventional Heated Humidity in Patients Suing Continuous Positive Airway Pressure

Further study details as provided by Fisher and Paykel Healthcare:

Primary Outcome Measures:
  • CPAP compliance [ Time Frame: 1, 4 & 8 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Subjective & objective sleep parameters [ Time Frame: 1, 4 & 8 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment:   80
Study Start Date:   August 2006
Estimated Study Completion Date:   May 2009
Estimated Primary Completion Date:   March 2009 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
B: Experimental
Heated breathing tube (CPAP with Thermosmart)
Device: Heated breathing tube (CPAP with ThermoSmart)
heated humidification with a heated breathing tube.
A: Active Comparator
Non heated breathing tube (CPAP with conventional humidification)
Device: Non heated breathing tube (CPAP with conventional humidification)
Heated humidification without a heated breathing tube

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  1. ≥ 18 years of age
  2. Previous diagnosis of OSA permitted, but patient must be novel to CPAP and no previous surgical intervention for OSA or treatment with an oral appliance.
  3. AHI ≥ 15 OR AHI ≥ 5 + ESS ≥ 10 OR ESS ≥ 10 + a medical co-morbidity
  4. Patient willing to give informed consent and follow study protocol.

Exclusion Criteria:

  1. Wake resting SpO2 < 90%
  2. Patient requires BiLevel PAP or supplemental oxygen
  3. The patient is medically unstable (e.g. respiratory or cardiac failure)
  4. Patient unwilling to give informed consent or follow study protocol.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00751335

Contacts
Contact: Judy Goodman, CCRC     847.981.3660     sla@sublung.com    

Locations
United States, Illinois
Suburban Lung Associates     Recruiting
      Chicago, Illinois, United States, 60007
      Principal Investigator: Clifford A Massie, PhD            

Sponsors and Collaborators
Fisher and Paykel Healthcare
Suburban Lung Associates

Investigators
Principal Investigator:     Clifford A Massie, PhD     Suburban Lung Asssociates    
  More Information


Suburban Lung Associates  This link exits the ClinicalTrials.gov site
 
Fisher & Paykel Healthcare  This link exits the ClinicalTrials.gov site
 
Chicago Sleep Group  This link exits the ClinicalTrials.gov site
 

Responsible Party:   Fisher & Paykel Healthcare ( Emma Duckworth/Clinical Research Manager )
Study ID Numbers:   FPHC SLA 2008
First Received:   September 10, 2008
Last Updated:   September 10, 2008
ClinicalTrials.gov Identifier:   NCT00751335
Health Authority:   United States: Food and Drug Administration

Keywords provided by Fisher and Paykel Healthcare:
Obstructive Sleep Apnea  
Humidification  
Continuous Positive Airway Pressure  

Study placed in the following topic categories:
Sleep Apnea Syndromes
Respiratory Tract Diseases
Apnea
Respiration Disorders
Sleep Apnea, Obstructive
Dyssomnias
Sleep Disorders
Sleep Disorders, Intrinsic

Additional relevant MeSH terms:
Nervous System Diseases

ClinicalTrials.gov processed this record on October 06, 2008




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