Clinical Trials Directory

Trials / Completed

CompletedNCT00910195

Validation of a New Automatic Bi-level Algorithm in the Treatment of Sleep-disordered Breathing

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Wissenschaftliches Institut Bethanien e.V · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Between 2%-4% of adult population suffers from obstructive sleep apnea (OSAS)(1), which is characterized by obstructive snoring, repetitive apnea and hypopnea in sleep, repetitive cyclic oxygen saturation, as a result from sleep fragmentation related to the arousals in sleeping profile and clinical consequences like day drowsiness, neuropsychological deficits, raised danger of accidents and cardiovascular disease. (1-6). The therapy of choice is the application of nasal continuous positive airway pressure (CPAP) (7-9). Increasing relevance obtain the combined sleep-related breathing disturbances, where the patient shows an obstructive sleep apnea syndrome and some central breathing disturbances in the polysomnography at night. Those patients frequently present with cardiovascular diseases. These combined night breathing disturbances are frequently insufficient to be mitigated exclusively with a CPAP therapy. Some modifications of nCPAP therapy were developed in order to optimize the therapy-compliance and the effectiveness of the therapy. Bi-level-CPAP-devices produce two pressure levels: one for inspiration and another for expiration, so that the patients are able expire against a constant low pressure. An increase in the use of this application in comparison between the conventional or the automatic CPAP therapy could not be proved in early studies. (12, 13) The principle of the automatic nCPAP therapy is to recognize the patient's current need of pressure and to alter the pressure within a set range by applying different algorithms. Some studies have shown that this therapy increased compliance and comfort (14-16), while other studies could not confirm these results. (17, 18) The result of the current study should prove if the treatment of a new algorithm therapy based on an automatic bi-level-system for patients with sleep-related respiratory disorders is as effectively and subjective more comfortable as the conventional CPAP therapy. Patients with a particularly high need of pressure should experience a clear expiratory pressure relief and a higher comfort. Therefore a better compliance is to expect. In the same way patients with additional central respiratory disturbances should obtain a benefit from the bi-level modus. This new treatment would help particularly such "critical patients", who are not responding well to the CPAP therapy or find it uncomfortable.

Detailed description

Patients who meet all the above mentioned criteria and who were diagnosed as sleep-apnea syndrome patients in our hospital were asked to participate in the study. By a declaration of consent the patients were randomized in two different groups. Group 1: started with CPAP at the first night and continued with Bi-level- APAP at the second night. Group 2: began with Bi-level-APAP and ended with CPAP Patients will be discharged with CPAP after the second night

Conditions

Interventions

TypeNameDescription
DEVICECPAP treatment with subsequent Bi-Level-APAP treatmentCPAP treatment during the first night and then Bi-level-APAP treatment during second night
DEVICEBi-Level-APAP treatment with subsequent CPAP treatmentBi-level-APAP treatment during the first night and then CPAP treatment during the second night

Timeline

Start date
2008-06-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2009-05-29
Last updated
2011-08-09

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00910195. Inclusion in this directory is not an endorsement.