Protein Synthesis in Midthigh Muscles PET/CT

NCT ID: NCT01008839

Last Updated: 2011-05-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to test a new imaging technique to help scientists study sarcopenia, the process by which muscle becomes weaker with age.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sarcopenia

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Old age group of healthy women

Old women over 70 years old

No interventions assigned to this group

young group of healthy women

aged 25-35 years

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* young healthy women aged 25-35 years and older healthy women above 70 years old.

Exclusion Criteria

* no cardiac disease, not taking medication for high blood pressure Asthma HIV any other cardiac conditions
Minimum Eligible Age

25 Years

Maximum Eligible Age

90 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of California, San Francisco

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

UCSF

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

TLANG_Protiensynthesis

Identifier Type: REGISTRY

Identifier Source: secondary_id

Protein Synthesis

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Pain in Fibrous Dysplasia
NCT04125862 COMPLETED NA