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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02324946
Other study ID # STOP-BANG, DES-OSA
Secondary ID
Status Completed
Phase N/A
First received December 19, 2014
Last updated June 28, 2017
Start date October 2014
Est. completion date December 2015

Study information

Verified date June 2017
Source Astes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The DES-OSA Score and the STOP-BANG score were predictive scores for Obstructive Sleep Apnea.

This study will compare, among patients scheduled for bariatric surgery, these two scores as predictive scores for a difficult intubation.


Description:

The DES-OSA Score and the STOP-BANG score were predictive scores for Obstructive Sleep Apnea.

This study will compare, among patients scheduled for bariatric surgery, these two scores as predictive scores for a difficult mask ventilation of tracheal intubation.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 2015
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- BMI > 30 kg m-2

- Preoperative Polysomnography

Exclusion Criteria:

- Pregnant women

- ENT Cancer

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mass Screening
Preoperative screening with STOP-BANG and DES-OSA scores and postoperative comparison with difficult intubation / ventilation scores.

Locations

Country Name City State
Belgium Clinique Saint-Luc de Bouge Bouge Namur

Sponsors (1)

Lead Sponsor Collaborator
Astes

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Predictive value of STOP-BANG and DES-OSA scores for difficult mask ventilation or intubation. 1 day
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