- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04644458
Use of Ulna Length to Predict Tidal Volume in Adult Egyptians
Use of Ulna Length to Predict Protective Lung Tidal Volume in Adult Egyptians
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
After approval of local ethical committee and informed consent, one hundred healthy volunteers will be rnrolled in this study. Height of each subject will be measured while standing upright against a wall. Then, the left ulna will be measured with a measure tape from the olecranon to mid point of styloid process. From ulna length, height is estimated as advised by Malnutrition Advisory Group, British Association of Parenteral and Enteral Nutrition. October 2008. Malnutrition Universal Screening Tool.Protective lung tidal volume is calculated as 6 ml/kg predicted body weight (PBW) as follow:
PBW= 50*0.91 (centimetres of height - 152.4) in males and 45.5*0.91(centimetres of height - 152.4) in females.
Each measurement will be performed only once for each subject. Agreement between measurements will be expressed by the Bland-Altman method.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Bahaa M Refaie, MD
- Phone Number: 01026887257
- Email: bahaarefaay@med.sohag.edu.eg
Study Locations
-
-
-
Sohag, Egypt
- Recruiting
- Sohag University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy adult Egyptian
Exclusion Criteria:
- Deformity or previous surgery in the left arm
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Protective lung tidal volume
Time Frame: measurement of left ulna while standing for each volunteer throught the study completion, average 6 months
|
measurement of left ulna while standing for each volunteer throught the study completion, average 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Hosam eldeen M Marie, MD, Consultant of anesthesia and ICU Elhelal insurance hospital
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1990 (CTEP)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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