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Long Term Vital Parameter Monitoring (LAVIMO) (LAVIMO)

Primary Purpose

Sleep Apnea, Obstructive

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
LAVIMO in- ear sensor system
Sponsored by
RWTH Aachen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Sleep Apnea, Obstructive focused on measuring Polysomnography, Long term vital signs monitoring, In-ear sensor system, Photoplethysmographic micro-optic device, High wearing comfort

Eligibility Criteria

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

Inclusion Criteria:

  • patients > 18 years who routinely have to undergo a polysomnography night
  • sleep apnoea patient
  • able to give informed consent

Exclusion Criteria:

  • dementia
  • cochlea implant
  • severe lung diseases
  • allergy against material of the sensor
  • inflammation of the middle ear
  • inflammation of auditory canal
  • occlusion because of cerumen
  • electric implants

Sites / Locations

  • Neurological Clinic , University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Device: in-ear sensor

Arm Description

Patients who routinely undergo a polysomnography night (1 night) are monitored via in-ear sensor which will be embedded in the auditory canal. During this night vital signs parameters are monitored, processed and subsequently compared to the polysomnography data.

Outcomes

Primary Outcome Measures

Extraction of vital signs out of measurement data via individually formed in-ear sensor system in comparison to standard polysomnography data in sleep laboratory
during one polysomnographic night in sleep laboratory the patient will receive the LAVIMO in- ear sensor system and vital parameters like heart rate, heart rate variability, breathing and oxygen saturation will be monitored. Subsequently the data will be processed and compared to the standard polysomnographic data

Secondary Outcome Measures

Full Information

First Posted
June 20, 2012
Last Updated
November 26, 2013
Sponsor
RWTH Aachen University
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1. Study Identification

Unique Protocol Identification Number
NCT01626274
Brief Title
Long Term Vital Parameter Monitoring (LAVIMO)
Acronym
LAVIMO
Official Title
Long Term Vital Parameter Monitoring Pilot Study to Evaluate Measurement Data Via In-ear Sensor in Comparison to Standard Polysomnography in Sleep Laboratory
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
February 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RWTH Aachen University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the feasibility of non-intrusive 24 hours non-invasive measurements with minimized LAVIMO sensor system. The LAVIMO-system is a photoplethysmographic device for reflective mode measurements of the optical damping upper skin layers inside of the ear canal at two different wave lengths. It consists of the in-ear sensor, the electronics and a PC. Vital signs parameter like heart rate, heart rate variability, breathing and arterial blood oxygenation are monitored in patients with sleep apnoea and compared to measurements of standard polysomnography of these patients during one night in the sleep laboratory.
Detailed Description
In 20 patients who routinely have to undergo a polysomnographic night in sleep laboratory LAVIMO measurements like heart rate, heart rate variability, breathing and arterial blood oxygenation are performed parallel to standard polysomnography measurements and subsequently compared to the data of the standard polysomnography. The LAVIMO sensor system consists of the in- ear sensor, the electronics and a PC; the individually formed sensor is embedded into an ear mould for proper fit inside the ear canal. Inside two LEDs emit light into the adjacent skin at 760 and 905 nm wavelengths. The intensity of the backscattered light is detected by a photo detector. In the electronics, the control signals for the LEDs are provided, as well as the photo detector signal is further processed and A-D converted. The electronics also provide a wireless connection to the PC via bluetooth. Data recording, post processing and displaying are tasks of the PC. The feasibility of non- intrusive 24 hours and non-invasive measurements like heart rate, heart rate variability, breathing and oxygen saturation is proved via this minimized sensor and electronics placed at a suitable place at the body guaranteeing high wearing comfort. This includes a wireless data communication for unrestricted mobility. Subsequently the data are compared to the standard polysomnography data to extract vital signs or for example to recognize possible phases of sleep apnoea. The goal in future refering to preventive medical monitoring will be early detection of risk factors for patient's health and improvement of living conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive
Keywords
Polysomnography, Long term vital signs monitoring, In-ear sensor system, Photoplethysmographic micro-optic device, High wearing comfort

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Device: in-ear sensor
Arm Type
Experimental
Arm Description
Patients who routinely undergo a polysomnography night (1 night) are monitored via in-ear sensor which will be embedded in the auditory canal. During this night vital signs parameters are monitored, processed and subsequently compared to the polysomnography data.
Intervention Type
Device
Intervention Name(s)
LAVIMO in- ear sensor system
Other Intervention Name(s)
Photoplethysmographic microoptic reflective microsensor
Intervention Description
Long term vital signs parameters like heart rate, heart rate variability, breathing and oxygen saturation are measured via in- ear sensor system during 1 polysomnographic night
Primary Outcome Measure Information:
Title
Extraction of vital signs out of measurement data via individually formed in-ear sensor system in comparison to standard polysomnography data in sleep laboratory
Description
during one polysomnographic night in sleep laboratory the patient will receive the LAVIMO in- ear sensor system and vital parameters like heart rate, heart rate variability, breathing and oxygen saturation will be monitored. Subsequently the data will be processed and compared to the standard polysomnographic data
Time Frame
one night

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients > 18 years who routinely have to undergo a polysomnography night sleep apnoea patient able to give informed consent Exclusion Criteria: dementia cochlea implant severe lung diseases allergy against material of the sensor inflammation of the middle ear inflammation of auditory canal occlusion because of cerumen electric implants
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johannes Schiefer, MD
Organizational Affiliation
Neurological Clinic, University Hospital Aachen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurological Clinic , University Hospital
City
Aachen
State/Province
North Rhine Westphalia
ZIP/Postal Code
52074
Country
Germany

12. IPD Sharing Statement

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Long Term Vital Parameter Monitoring (LAVIMO)

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