NCT04644458

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2020

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 20, 2020

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

November 15, 2020

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 25, 2020

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2023

Completed
Last Updated

September 28, 2021

Status Verified

September 1, 2021

Enrollment Period

2.6 years

First QC Date

November 15, 2020

Last Update Submit

September 26, 2021

Conditions

Tidal Volume

Outcome Measures

Primary Outcomes (1)

  • Protective lung tidal volume

    measurement of left ulna while standing for each volunteer throught the study completion, average 6 months

Interventions

Measuring the ulna length using meauring tapeOTHER

the left ulna will be measured with a measure tape from the olecranon to mid point of styloid process.

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Adult Egyptian volunteers

You may qualify if:

  • \- Healthy adult Egyptian

You may not qualify if:

  • \- Deformity or previous surgery in the left arm

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sohag university hospital

Sohag, Egypt

RECRUITING

Study Officials

  • Hosam eldeen M Marie, MD

    Consultant of anesthesia and ICU Elhelal insurance hospital

    STUDY DIRECTOR

Central Study Contacts

Bahaa M Refaie, MD

CONTACT

01026887257bahaarefaay@med.sohag.edu.eg

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of anesthesia and ICU

Study Record Dates

First Submitted

November 15, 2020

First Posted

November 25, 2020

Study Start

October 20, 2020

Primary Completion

June 1, 2023

Study Completion

July 1, 2023

Last Updated

September 28, 2021

Record last verified: 2021-09

Locations

EG(1)