Comparison of Demographic Data Mentioned by the Patients or Measured by a Physician

April 22, 2024 updated by: Eric DEFLANDRE, MD, PhD, FCCP, FAHA, FAACD, Astes
OSA (Obstructive Sleep Apnea) represents a major risk of postoperative complications. Predictive scores have been developed as the STOP-Bang score and the DES-OSA score. These scores take into account morphological parameters such as weight, height, and neck circumference. These data can be contained from the patients (self-reported) or by the measurements performed by a physician. The aim of this study is to compare the accuracy of both measurements (self-reported by the patient or measured by the physicians).

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

187

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Belgium
      • Namur, Belgium, 5004
        • Clinique Saint-Luc Bouge

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

All patients included

Description

Inclusion Criteria:

  • All patients scheduled for elective surgery on a one-day hospital

Exclusion Criteria:

  • Patient refusal

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Study group
All patients included in this study. Investigators will record both self-reported and measured height, weight, and neck circumference in all of these patients.
Other: Self-reported
Self-reported height, weight, and neck circumference
Other: Measured
Height, weight, and neck circumference measured by the investigator.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accuracy of self-reported height measurements
Time Frame: One month
The aim of this study is to determine the accuracy of the self-reported height (compared to height measured by the physician).
One month
Accuracy of self-reported weight measurements
Time Frame: One month
The aim of this study is to determine the accuracy of the self-reported weight (compared to height measured by the physician).
One month
Accuracy of self-reported neck circumference measurements
Time Frame: One month
The aim of this study is to determine the accuracy of the self-reported neck circumference (compared to height measured by the physician).
One month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Astes

Investigators

  • Principal Investigator: Eric Deflandre, MD, PhD, Astes

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2023

Primary Completion (Actual)

September 30, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

January 24, 2023

First Submitted That Met QC Criteria

February 1, 2023

First Posted (Actual)

February 2, 2023

Study Record Updates

Last Update Posted (Actual)

April 23, 2024

Last Update Submitted That Met QC Criteria

April 22, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PTS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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