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NCT06457165Completed

The Role of Anthropometric Measurements and Ultrasonograpic Suprasternal Adipose Tissue Thickness

Predicting Difficult Intubation in Obese Patients: The Role of Anthropometric Measurements and Ultrasonograpic Suprasternal Adipose Tissue Thickness

Source: ClinicalTrials.gov · Last updated 14 Jun 2024

Brief summary (registry, in English)

Prediction of difficult preoperative intubation in obese patients and completion of preparations for difficult intubation both reduce the risk of repeated intubation and prevent complications. In this study, the investigators aimed to evaluate whether anthropometric measurements are superior in defining difficult preoperative airways.

Status (registry)
Completed
Study type
Observational
Enrollment
40 (actual)
First submitted
10 Jun 2024
Start date
1 Jan 2021
Primary completion date
1 Jan 2022
Lead sponsor
Ankara City Hospital Bilkent
Diseases
Obesity
NCT number
NCT06457165

What you commit to

  • Study type: Observational
  • Participants enrolled: 40
  • From 1 Jan 2021 to the primary completion date, 1 Jan 2022
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • \<18 and \>60 years

Other

  • ASA\>3
  • BMI\<30

Who the study is looking for

  • 18-60 years
  • ASA 1-3
  • BMI ≥30 kg/m2
  • ASA 1-3
  • Scheduled for elective abdominal surgery under general anesthesia

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ankara Bilkent City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.