search
Back to results

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

Primary Purpose

Obstructive Sleep Apnea

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
CPAP treatment with subsequent Bi-Level-APAP treatment
Bi-Level-APAP treatment with subsequent CPAP treatment
Sponsored by
Wissenschaftliches Institut Bethanien e.V
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea focused on measuring Obstructive sleep apnea, CPAP, Bi-Level

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women > 18 years.
  • Newly diagnosed of sleep-apnea-syndrome, AHI> 5 per hour associated with the usual manifestation of this syndrome.
  • Declaration of consent.

Exclusion Criteria:

  • Absence of declaration of consent.
  • Other relevant sleep disorders like insomnia, restless legs, parasomnia
  • Heart failure NYHA-CLASS III- IV.
  • Myocardial infarction or unstable angina pectoris or cardiac surgery in within the last three months.
  • Apnea-hypopnea-index < 5 per hour.
  • Pregnancy.
  • Malign diseases.
  • Serious chronic oxygen-requiring pulmonary illness.
  • Age under 18 years.

Sites / Locations

  • Wissenschaftliches Institut Bethanien e.V.

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

CPAP before Bi-Level-APAP

Bi-Level-APAP before CPAP

Arm Description

receiving CPAP treatment during the first night and then Bi-level-APAP treatment during second night

receiving Bi-level-APAP treatment during the first night and then CPAP treatment during the second night

Outcomes

Primary Outcome Measures

Obstructive and central apnea-hypopnea-Index.

Secondary Outcome Measures

Total apnea-hypopnea-index, minimum and middle oxygen saturation, subjective satisfaction with the therapy (questionnaire).

Full Information

First Posted
May 28, 2009
Last Updated
August 8, 2011
Sponsor
Wissenschaftliches Institut Bethanien e.V
search

1. Study Identification

Unique Protocol Identification Number
NCT00910195
Brief Title
Validation of a New Automatic Bi-level Algorithm in the Treatment of Sleep-disordered Breathing
Official Title
Validation of a New Automatic Bi-level Algorithm in the Treatment of Sleep-disordered Breathing
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
June 2008 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Wissenschaftliches Institut Bethanien e.V

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea
Keywords
Obstructive sleep apnea, CPAP, Bi-Level

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CPAP before Bi-Level-APAP
Arm Type
Experimental
Arm Description
receiving CPAP treatment during the first night and then Bi-level-APAP treatment during second night
Arm Title
Bi-Level-APAP before CPAP
Arm Type
Experimental
Arm Description
receiving Bi-level-APAP treatment during the first night and then CPAP treatment during the second night
Intervention Type
Device
Intervention Name(s)
CPAP treatment with subsequent Bi-Level-APAP treatment
Intervention Description
CPAP treatment during the first night and then Bi-level-APAP treatment during second night
Intervention Type
Device
Intervention Name(s)
Bi-Level-APAP treatment with subsequent CPAP treatment
Intervention Description
Bi-level-APAP treatment during the first night and then CPAP treatment during the second night
Primary Outcome Measure Information:
Title
Obstructive and central apnea-hypopnea-Index.
Time Frame
day one and two of the study
Secondary Outcome Measure Information:
Title
Total apnea-hypopnea-index, minimum and middle oxygen saturation, subjective satisfaction with the therapy (questionnaire).
Time Frame
day one and two of the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women > 18 years. Newly diagnosed of sleep-apnea-syndrome, AHI> 5 per hour associated with the usual manifestation of this syndrome. Declaration of consent. Exclusion Criteria: Absence of declaration of consent. Other relevant sleep disorders like insomnia, restless legs, parasomnia Heart failure NYHA-CLASS III- IV. Myocardial infarction or unstable angina pectoris or cardiac surgery in within the last three months. Apnea-hypopnea-index < 5 per hour. Pregnancy. Malign diseases. Serious chronic oxygen-requiring pulmonary illness. Age under 18 years.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wolfgang Galetke, PD Dr.
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Winfried J. Randerath, Prof. Dr.
Official's Role
Study Director
Facility Information:
Facility Name
Wissenschaftliches Institut Bethanien e.V.
City
Solingen
State/Province
NRW
ZIP/Postal Code
42699
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
11208620
Citation
Shahar E, Whitney CW, Redline S, Lee ET, Newman AB, Nieto FJ, O'Connor GT, Boland LL, Schwartz JE, Samet JM. Sleep-disordered breathing and cardiovascular disease: cross-sectional results of the Sleep Heart Health Study. Am J Respir Crit Care Med. 2001 Jan;163(1):19-25. doi: 10.1164/ajrccm.163.1.2001008.
Results Reference
background
PubMed Identifier
8464434
Citation
Young T, Palta M, Dempsey J, Skatrud J, Weber S, Badr S. The occurrence of sleep-disordered breathing among middle-aged adults. N Engl J Med. 1993 Apr 29;328(17):1230-5. doi: 10.1056/NEJM199304293281704.
Results Reference
background
PubMed Identifier
11286346
Citation
Finn L, Young T, Palta M, Fryback DG. Sleep-disordered breathing and self-reported general health status in the Wisconsin Sleep Cohort Study. Sleep. 1998 Nov 1;21(7):701-6.
Results Reference
background
PubMed Identifier
10893080
Citation
Engleman HM, Kingshott RN, Martin SE, Douglas NJ. Cognitive function in the sleep apnea/hypopnea syndrome (SAHS). Sleep. 2000 Jun 15;23 Suppl 4:S102-8.
Results Reference
background
PubMed Identifier
15333860
Citation
George CF. Sleep. 5: Driving and automobile crashes in patients with obstructive sleep apnoea/hypopnoea syndrome. Thorax. 2004 Sep;59(9):804-7. doi: 10.1136/thx.2003.007187.
Results Reference
background
PubMed Identifier
11254519
Citation
Randerath WJ, Schraeder O, Galetke W, Feldmeyer F, Ruhle KH. Autoadjusting CPAP therapy based on impedance efficacy, compliance and acceptance. Am J Respir Crit Care Med. 2001 Mar;163(3 Pt 1):652-7. doi: 10.1164/ajrccm.163.3.2006168.
Results Reference
background
PubMed Identifier
12942031
Citation
Randerath WJ, Galetke W, Ruhle KH. Auto-adjusting CPAP based on impedance versus bilevel pressure in difficult-to-treat sleep apnea syndrome: a prospective randomized crossover study. Med Sci Monit. 2003 Aug;9(8):CR353-8.
Results Reference
background

Learn more about this trial

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

We'll reach out to this number within 24 hrs