Radiological Evaluation of Sarcopenia in Patient Received Chemotherapy
1 other identifier
observational
72
0 countries
N/A
Brief Summary
Radiological evaluation of sarcopenia in patients receiving chemotherapy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 2, 2023
CompletedFirst Posted
Study publicly available on registry
December 12, 2023
CompletedStudy Start
First participant enrolled
January 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2025
CompletedDecember 12, 2023
December 1, 2023
1.2 years
December 2, 2023
December 8, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Radiological evaluation of sarcopenia in patients receiving chemotherapy
Using sonoelastography and computed tomography in evaluation of muscle mass in patients received chemotherapy by measurement of muscle thickness ,echogencity ,cross sectional area ,fasicle length,pennation angle, strain ratio,shear wave velocity
April 2025
Eligibility Criteria
Comparison of muscle mass before and after chemotherapy by use of sonoelastography and computed tomography and comparison with normal volunteer
You may qualify if:
- all cancer patients receiving chemotherapy referred to radiodiagnosis department for routine examination Patients must be between 18 and
You may not qualify if:
- Previous or current history of any musculoskeletal or neurological disorder including strokes.
- Systemic atrophy affecting CNS ( Huntington disease ,hereditary ataxia ,spinal muscular disorder and related syndromes ,post polio syndrome )
- Central nervous system demyelinating disease ( Multiple sclerosis , acute disseminated demyelinated syndromes..
- Corticosteroids undertaken currently or for the past 3 years with doses \>5mg/day.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Lamiaa Refaat, Assisstant professor
Assiut university -south egypt cancer institute
- STUDY DIRECTOR
Omar Mostafa, Assisstant professor
Assiut university -south egypt cancer institute
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident doctor
Study Record Dates
First Submitted
December 2, 2023
First Posted
December 12, 2023
Study Start
January 1, 2024
Primary Completion
April 1, 2025
Study Completion
April 1, 2025
Last Updated
December 12, 2023
Record last verified: 2023-12