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COMPLETED NA

Titration Pressures in Sleep Apnea Patients Using ThermoSmart® Versus Conventional Humidification

NCT00681083 · View on ClinicalTrials.gov ↗

Study Summary

Patients who have Obstructive Sleep Apnea (OSA) may have different Continuous Positive Airway Pressure (CPAP)when titrated with different levels of humidification. It is hypothesised that patients with ThermoSmart® technology (heated breathing tube technology) will have lower titrated pressures than those who are titrated using conventional humidification (non heated breathing tube).

Conditions Studied

Interventions

  • DEVICE Heated breathing tube (CPAP with ThermoSmart)
  • DEVICE Non heated breathing tube (CPAP with conventional humidification)

Study Locations (2)

Oklahoma

  • Sleep Center of Tulsa - Midtown — Tulsa
  • Sleep Center of Tulsa - South — Tulsa

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2008-04
Est. Completion 2008-07
Phase NA

Sponsor

Fisher and Paykel Healthcare

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00681083

The ClinicalTrials.gov registry entry for NCT00681083 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Fisher and Paykel Healthcare, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Sleep Apnea, Obstructive appearing as the primary indexed condition, and to 2 interventions — of which Heated breathing tube (CPAP with ThermoSmart) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00681083 reports 2 study locations spanning 1 distinct geographic area — top geographies include Oklahoma. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00681083 about?

NCT00681083 is a clinical study titled "Titration Pressures in Sleep Apnea Patients Using ThermoSmart® Versus Conventional Humidification". Patients who have Obstructive Sleep Apnea (OSA) may have different Continuous Positive Airway Pressure (CPAP)when titrated with different levels of humidification. It is hypothesised that patients with ThermoSmart® technology (heated breathing tube technology) will have lower titrated pressures than...

What is the current status of trial NCT00681083?

This trial is currently completed. It is a NA study. The enrollment target is 26 participants. The study started on 2008-04. Estimated completion is 2008-07.

What conditions does trial NCT00681083 study?

This clinical trial studies the following conditions: Sleep Apnea, Obstructive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00681083?

The interventions under investigation include: Heated breathing tube (CPAP with ThermoSmart) (DEVICE), Non heated breathing tube (CPAP with conventional humidification) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00681083?

This trial is sponsored by Fisher and Paykel Healthcare, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00681083 being conducted?

This trial has 2 study locations across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial