Respiratory Failure Clinical Trial
Official title:
Automated Oxygen Delivery by O2matic to Patients Admitted With an Exacerbation in COPD
The aim of the study is to examine if automated oxygen delivery with O2matic is better than
manually controlled oxygen therapy for patients admitted to hospital with an exacerbation in
Chronic Obstructive Pulmonary Disease (COPD).
O2matic is a closed -loop system based on continuous non-invasive measurement of pulse and
oxygen-saturation that is processed in an algorithm that controls the flow of oxygen to the
patient.
The primary hypothesis is that O2matic increases time within acceptable oxygen-saturation
interval. Secondary hypotheses are that O2matic compared to manual control reduces time with
severe hypoxia (SpO2 < 85 %), hypoxi (SpO2 below intended interval) and hyperoxia (SpO2 above
intended interval).
Closed-loop control of oxygen therapy is described in the literature used for preterm
infants, trauma patients, medical emergency use and patients with COPD. For the latter,
closed-loop therapy has been used for patients admitted to hospital with an exacerbation, for
domiciliary oxygen use and during exercise. O2matic is a closed-loop system that is based on
continuous and non-invasive measurement of pulse, oxygen-saturation and respiratory
frequency. The algorithm in O2matic controls oxygen delivery with the aim of keeping the
saturation within the desired interval, which could be 88-92 % for COPD-patients in
accordance with international guidelines on this topic. Saturation interval can be set for
the individual patients, as can the range of acceptable oxygen-flow. If saturation or
oxygen-flow can't be maintained within the desired intervals an alarm will sound.
All studies on closed-loop systems have shown that this method is better than manually
control by nurse to maintain saturation within the desired interval. Furthermore, some
studies have indicated that closed-loop has the possibility to reduce admission time and to
reduce time spent with oxygen therapy, due to more efficient and fast withdrawal from oxygen
supplementation.
In the present study O2matic will be tested versus manual control, for patients admitted with
an exacerbation in COPD, and in need of supplemental oxygen. During the study the patients
will either have oxygen controlled with O2matic or manually by nursing staff. All patients
will have continuous logging of pulse, oxygen-saturation and oxygen-flow with O2matic, but
only in the O2matic active group, the algorithm will control oxygen-delivery.
The primary hypothesis will be tested, which is that O2matic is better than manual control
for maintaining oxygen-saturation within the desired interval and reducing time with
unintended hypoxia and hyperoxia. For this purpose 20 patients will be included in a
crossover design with 4 hours of O2matic-controlled oxygen treatment and 4 hours with
manually titrated oxygen with a 16 hours washout between periods.
No safety issues has been reported in the literature. Before use O2matic will be approved by
The Danish Medicines Agency, The Ethics Committee in the Capital Region of Denmark and by the
regional Data Protection Board. The study will be conducted according to GCP standards with
independent monitoring. All adverse events and serious adverse events will be monitored and
serious adverse events will be reported to Danish Medicines Agency.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03909854 -
Pragmatic Investigation of Volume Targeted Ventilation-1
|
N/A | |
Recruiting |
NCT03662438 -
HOPE (Home-based Oxygen [Portable] and Exercise) for Patients on Long Term Oxygen Therapy (LTOT)
|
N/A | |
Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
Recruiting |
NCT05535543 -
Change in the Phase III Slope of the Volumetric Capnography by Prone Positioning in Acute Respiratory Distress Syndrome
|
||
Completed |
NCT04030208 -
Evaluating Safety and Efficacy of Umbulizer in Patients Requiring Intermittent Positive Pressure Ventilation
|
N/A | |
Recruiting |
NCT04542096 -
Real Time Evaluation of Dynamic Changes of the Lungs During Respiratory Support of VLBW Neonates Using EIT
|
||
Recruiting |
NCT04668313 -
COVID-19 Advanced Respiratory Physiology (CARP) Study
|
||
Recruiting |
NCT05883137 -
High-flow Nasal Oxygenation for Apnoeic Oxygenation During Intubation of the Critically Ill
|
||
Completed |
NCT04505592 -
Tenecteplase in Patients With COVID-19
|
Phase 2 | |
Completed |
NCT03943914 -
Early Non-invasive Ventilation and High-flow Nasal Oxygen Therapy for Preventing Delayed Respiratory Failure in Hypoxemic Blunt Chest Trauma Patients.
|
N/A | |
Active, not recruiting |
NCT03472768 -
The Impact of Age-dependent Haptoglobin Deficiency on Plasma Free Hemoglobin Levels During Extracorporeal Membrane Oxygenation Support
|
||
Not yet recruiting |
NCT04538469 -
Absent Visitors: The Wider Implications of COVID-19 on Non-COVID Cardiothoracic ICU Patients, Relatives and Staff
|
||
Not yet recruiting |
NCT02542423 -
Endocan Predictive Value in Postcardiac Surgery Acute Respiratory Failure.
|
N/A | |
Completed |
NCT02265198 -
Relationship of Pulmonary Contusion to Pulmonary Inflammation and Incidence of Acute Respiratory Distress Syndrome
|
N/A | |
Completed |
NCT02105298 -
Effect of Volume and Type of Fluid on Postoperative Incidence of Respiratory Complications and Outcome (CRC-Study)
|
N/A | |
Completed |
NCT01885442 -
TryCYCLE: A Pilot Study of Early In-bed Leg Cycle Ergometry in Mechanically Ventilated Patients
|
N/A | |
Completed |
NCT02814994 -
Respiratory System Compliance Guided VT in Moderate to Severe ARDS Patients
|
N/A | |
Completed |
NCT01659268 -
Performance of Baccalaureate Nursing Students in Insertion of Laryngeal Mask: a Trial in Mannequins
|
N/A | |
Terminated |
NCT01333059 -
Cycling of Sedative Infusions in Critically Ill Pediatric Patients
|
N/A | |
Completed |
NCT01204281 -
Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients
|
Phase 4 |