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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04644458
Other study ID # 1990
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 20, 2020
Est. completion date July 2023

Study information

Verified date September 2021
Source Sohag University
Contact Bahaa M Refaie, MD
Phone 01026887257
Email bahaarefaay@med.sohag.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to evaluate the ability of ulna length to predict accurate protective lung tidal volume in Egyptian people in reference to their standing height.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 2023
Est. primary completion date June 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Healthy adult Egyptian Exclusion Criteria: - Deformity or previous surgery in the left arm

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Measuring the ulna length using meauring tape
the left ulna will be measured with a measure tape from the olecranon to mid point of styloid process.

Locations

Country Name City State
Egypt Sohag university hospital Sohag

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Protective lung tidal volume measurement of left ulna while standing for each volunteer throught the study completion, average 6 months
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