- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02766504
Ultrasound in Airway Assessment of Morbidly Obese Patients (AiUs)
May 5, 2016 updated by: AlRefaey Kandeel, Mansoura University
the study aims to evaluate the role of airway ultrasound as a new evolving modality in assessment and management of airway in surgical patients
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
100
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
-
-
Dkahleya
-
Mansoura, Dkahleya, Egypt
- Recruiting
- Mansoura University
-
Contact:
- Alreafey Kandeel, MD
- Phone Number: 00201008158591
- Email: refa3ey2@yahoo.com
-
-
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
20 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
surgical list patients with indicated endotracheal tube insertion for general anesthesia
Description
Inclusion Criteria:
- all surgical list patients planned for general anesthesia from october 2015 to may 2016
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
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prediction of difficult intubation in morbid obese patients
Time Frame: during endotracheal tube insertion
|
prediction of difficult intubation in morbid obese versus traditional airway scores; Mallampati score.
|
during endotracheal tube insertion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
October 1, 2015
Primary Completion (Anticipated)
May 1, 2016
Study Completion (Anticipated)
June 1, 2016
Study Registration Dates
First Submitted
October 3, 2015
First Submitted That Met QC Criteria
May 5, 2016
First Posted (Estimate)
May 9, 2016
Study Record Updates
Last Update Posted (Estimate)
May 9, 2016
Last Update Submitted That Met QC Criteria
May 5, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- refa 7 105
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.