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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02909309
Other study ID # P2016/329
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date July 31, 2017

Study information

Verified date August 2018
Source Erasme University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of a Mandibular and Abdominal Motion Detection Sensor (JAWAC) to Prevent Apnea During Sedation With Propofol in TCI Mode


Description:

In 2016 , monitoring of propofol sedation , currently recommended by the American Society of Anaesthesiology and European companies includes among others, a pulse oximeter (SpO2) and a continuous measurement of CO2 exhaled by an appropriate device (CapnoLine). This monitoring does not allow to anticipate the occurrence of obstructive apnea .

The anticipation of the occurrence of apnea or airway obstruction using this type of monitoring could allow the anesthesiologist to act earlier on the titration of propofol and maintaining the airway. This would avoid the side effects associated with hypoxemia and hypercapnia and therefore further improve patient safety .

This pilot study tests the JAWAC system to detect those apneas.

This is an interventional diagnostic study on the JAWAC monitoring system validation in a prospective cohort of patients undergoing sedation in order to provoke sleep apnea. Indeed , sedation technique is already used with propofol during snoring provocation tests in patients at risk for sleep apnea.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date July 31, 2017
Est. primary completion date July 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Any adult patient scheduled for a sleep apnea provocation test under sedation by propofol

- Hospital Erasme during the period of the study.

Exclusion Criteria:

1. Patient Refusal

2. Patient Age: 18 years and under 80 years

3. Intervention earlier in the mandible or thorax

4. A history of facial burn

5. Allergy tape

Study Design


Related Conditions & MeSH terms


Intervention

Device:
JAWAC system + Capnoline + Spo2
measure mandibular mouvements + etCO2 + pulse oxymetry, respectively

Locations

Country Name City State
Belgium Erasme Hospital Brussels

Sponsors (1)

Lead Sponsor Collaborator
Erasme University Hospital

Country where clinical trial is conducted

Belgium, 

References & Publications (3)

Niklewski PJ, Phero JC, Martin JF, Lisco SJ. A novel index of hypoxemia for assessment of risk during procedural sedation. Anesth Analg. 2014 Oct;119(4):848-56. doi: 10.1213/ANE.0000000000000371. — View Citation

Senny F, Destiné J, Poirrier R. Midsagittal jaw movement analysis for the scoring of sleep apneas and hypopneas. IEEE Trans Biomed Eng. 2008 Jan;55(1):87-95. doi: 10.1109/TBME.2007.899351. — View Citation

Tinker JH, Dull DL, Caplan RA, Ward RJ, Cheney FW. Role of monitoring devices in prevention of anesthetic mishaps: a closed claims analysis. Anesthesiology. 1989 Oct;71(4):541-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Optimal JAWAC signal threshold detecting obstructive apnea The apnea is defined clinically by the anesthesiologist with the help of the capnoLine/Spo2. The purpose is to define the optimal signal detection during a continuous record of the system JAWAC associated with the occurrence of obstructive apnea.
The results will give a variation in centimeters for a certain amount of time. It is possible that the optimal signal detection will be a combination of different sensors.
The sensibility, specificity versus precocity of the signal will be studied.
at time of anesthesia
Secondary Time limit between the detection of each system and the episode of désaturation The assumption is that the signal JAWAC enable an earlier response of the anesthetist and a priori reduce the occurrence of desaturation at the onset of obstructive apnea compared to the capnoLine/spo2 system. at time of anesthesia
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