L1 M1 of LDCT for Low Muscle Mass Measurement
Sponsor
Far Eastern Memorial Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04547478
Collaborator
(none)
3,304
1
17.6
187.6
Study Details
Study Description
Brief Summary
The first lumbar spine muscle index (L1 MI) on computed tomography (CT) obtained by measuring muscle surface at the first lumbar vertebrae (L1) level is an indicator of total skeletal mass in specific populations. Nevertheless, the utility of L1 MI derived from low dose chest CT (LDCT) in health assessments and relevant cutoff points are unclear.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
3304 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Evaluation of Low Muscle Mass by Muscle Surface Index of First Lumbar Vertebrae Using Low Dose Computed Tomography
Actual Study Start Date
:
Jan 21, 2019
Actual Primary Completion Date
:
Apr 20, 2020
Actual Study Completion Date
:
Jul 10, 2020
Outcome Measures
Primary Outcome Measures
- Cross sectional muscle area of the 1st vertebrae level [52 weeks]
Cross sectional muscle area of the 1st vertebrae level by LDCT
Eligibility Criteria
Criteria
Ages Eligible for Study:
20 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- Adults older than 20 years who received LDCT in routine health assessments from January to December 2017 were enrolled at a tertiary care hospital (Far Eastern Memorial Hospital, New Taipei City, Taiwan).
Exclusion Criteria:
- nil
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Far Eastern Memorial Hospital | New Taipei | Taiwan | 220 |
Sponsors and Collaborators
- Far Eastern Memorial Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Far Eastern Memorial Hospital
ClinicalTrials.gov Identifier:
NCT04547478
Other Study ID Numbers:
- IRB-107091-E
First Posted:
Sep 14, 2020
Last Update Posted:
Sep 14, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: