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SarcopeniaNCT06166134

Radiological Evaluation of Sarcopenia in Patient Received Chemotherapy

An observational study of Sarcopenia, run by Assiut University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Radiological evaluation of sarcopenia in patients receiving chemotherapy Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Sarcopenia
How many people
72 participants
Where
No sites listed yet
Study dates
Jan 2024to Apr 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Comparison of muscle mass before and after chemotherapy by use of sonoelastography and computed tomography and comparison with normal volunteer

Who may be able to join

  • all cancer patients receiving chemotherapy referred to radiodiagnosis department for routine examination Patients must be between 18 and

Who cannot join

  • 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.

Trial locations and contacts

No sites are listed yet.

Doaa Maher ebied Maher, Resident contact

01050147500

dm953407@gmail.com

Hasan ibrahim Megally, Professor contact

01006209584

Hasanibrahim48@yahoo.com

About this study

Radiological evaluation of sarcopenia in patients receiving chemotherapy

Read the detailed description

Evaluation of muscle mass by using sonoelastography and computed tomography

Conditions
Sarcopenia
Medical subject headings
Sarcopenia

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: April 2025

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Dec 2023
  2. Study startJan 2024 (estimated)
  3. Primary completionApr 2025 (estimated)
  4. Study completionApr 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
72 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06166134
Sponsor's protocol ID
Us and CT in sarcopenia
Status last verified
Dec 2023
First submitted
2 Dec 2023
Last updated
12 Dec 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Sarcopenia, run by Assiut University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 12 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Doaa Maher ebied Maher, Resident (01050147500, dm953407@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Radiological evaluation of sarcopenia in patients receiving chemotherapy (time frame: April 2025). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2023; AzTrials last refreshed its copy on 7 Nov 2026.

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