Skip to content

Evaluation of Safety and Efficacy of Shorttime TNI Treatment in Patients With COPD

STIT-1 Evaluation of Safety and Efficacy of Shorttime TNI Treatment in Patients With COPD

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01686893
Acronym
STIT-1
Enrollment
50
Registered
2012-09-18
Start date
2009-02-28
Completion date
2013-03-31
Last updated
2012-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oxygen Inhalation Therapy

Keywords

Oxygen, Insufflation, COPD, High Flow Treatment

Brief summary

Evaluation of Safety and Efficacy of Shorttime TNI Treatment in Patients with COPD Acute testing of oxygen demand using TNI vs. standard oxygen application in stable COPD patients An investigator-initiated, prospective, controlled, multicenter study

Detailed description

TNI, the nasal insufflation of a high flow of warm, humidified air, is an extremely comfortable and uncomplicated alternative to numerous other approaches in non-invasive ventilation (NIV). Up to now, NIV therapy could only be applied by masks with the associated complications as patients could not tolerate high airflow delivered by a thin nasal cannula without humidification and warming, thus causing concomitant negative effects. The new therapy TNI shows a high rate of acceptance by children, too. At present, there are two different types of devices available for nasal insufflation in clinics: TNI 20s, an air humidifier for clinical compressed air, and the TNI20 oxy, an air humidifier for clinical compressed air, which can be combined with oxygen. TNI 20 oxy The system, which is unique throughout the world, is optimized for the application of flows of up to 20L/min and fulfils the minimum requirements of the American Society of Testing and Materials for a high flow air humidifier in the non-invasive application of 10 mg H2O/L (equivalent to about 60% rel. humidity at an ambient temperature of 22°C) for the air humidity. The warming of the air flow by 5-15°C can be adjusted relative to the ambient temperature. Condensation is prevented in the nasal applicator by heating the tube as far as the nostrils. The device automatically controls humidity and temperature depending on the prevailing ambient conditions. The TNI®20s can be attached to the hospital infrastructure by means of a standard pressure regulator.

Interventions

DEVICENasal oxygen insufflation with a TNI 20 oxy device

Nasal oxygen insufflation with a TNI 20 oxy device

DEVICEStandard Nasal Insufflation of oxygen

Standard Nasal Insufflation of oxygen

Sponsors

Medical University Innsbruck
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

\- COPD patients with an indication for long-term oxygen therapy Age 30 - 80 years COPD GOLD °III

Exclusion criteria

\- Clinical instability of the patient No lung function testing possible Exacerbation within the last 14 days prior to inclusion into the study Serious concomitant diseases that may jeopardize the inclusion of the patient into the study from the investigator's point of view Anaemia, defined by a haemoglobin \<10 G/L Patients with hypercapnia, defined by a paCO \<46mmHg Participation of the patient in any other ongoing study

Design outcomes

Primary

MeasureTime frameDescription
PaO2Measures at Baseline and after 60 minChange in the partial oxygen pressure in the arterial blood (blood gas analysis) at a defined oxygen flow rate (L/min)

Secondary

MeasureTime frameDescription
O2 %Measures at Baseline and after 60 minChange in the oxygen saturation in the arterial blood (blood gas analysis) at a defined oxygen flow rate (L/min)
PaCO2Measures at Baseline and after 60 minChange in the partial carbon dioxide pressure in the arterial blood (blood gas analysis) at a defined oxygen flow rate (L/min)
AaDO2Measures at Baseline and after 60 minChange in the AaDO2 in the peripheral blood at a defined oxygen flow rate (L/min)
RV and TLCMeasures at Baseline and after 60 minSafety of the device in COPD °III or IV patients: No increase in the residual volume (RV) and the total lung capacity (TLC) \> 15% of the mean actual value at visits 1 and 2 (measurement 60 + 10 minutes after oxygen insufflation with a TNI system).

Countries

Austria, Germany, Switzerland

Contacts

Primary ContactChristian M Kaehler, MD
c.m.kaehler@i-med.ac.at004351250423255

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026