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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02089971
Other study ID # BL23
Secondary ID
Status Completed
Phase N/A
First received March 14, 2014
Last updated January 16, 2015
Start date March 2014
Est. completion date December 2014

Study information

Verified date January 2015
Source Abbott Nutrition
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

To describe the normal range of muscle mass and function in Chinese adults.


Description:

The study objective is to setup a normal range of muscle mass and function in Chinese adults.


Recruitment information / eligibility

Status Completed
Enrollment 412
Est. completion date December 2014
Est. primary completion date October 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years to 34 Years
Eligibility Inclusion Criteria:

1. Young adult ages between 25 and 34 years, inclusively.

2. Adult is judged to be in good health as determined from his/her medical history as his/her self-report to the enrolling center personnel and as confirmed through a clinical examination by a physician.

3. Adult with BMI between 18.5 to 26.9.

4. Male or non-pregnant non-lactating female. Non-pregnant should be confirmed by urine pregnant test. And non-lactating is defined as postpartum more than 18 months.

5. Subject has voluntarily signed and dated an informed consent form, approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) prior to any participation in the study.

Exclusion Criteria:

1. Subject who is heavy manual labor.

2. Subject who is professional or semi-professional athlete or game player.

3. Subject who is physical disabilities, such as loss of hand or foot or limbs or any physical disability which may affect the physical activities and affect the distribution of muscle mass by the opinion of the study physician.

4. Subject has known chronic diseases such as endocrine system diseases (including type 1 or type 2 diabetes mellitus, or hyperthyroidism or hypothyroidism), cardiovascular diseases, liver diseases, and renal diseases as self-report.

5. Subject who has active infection of TB, HIV and hepatitis as self-report.

6. Subject who currently experiencing diarrhea or anorexia within 7days prior to the enrollment.

7. Subject who has or plans for intensive physical activities 3 days prior to the scheduled BIA measurement.

8. Subject who is thyroid malfunction (as serum fT4 level and/or serum TSH level out of the reference range of the lab)

9. Subject has implanted electronic device, orthopedic metal implantations, such as pacemaker, cardiac defibrillator, or metal hip, metal knee joint, metal fracture internal fixation, etc.

10. Subject is drug addiction or alcohol addiction.

11. Subject is anemia (as blood hemoglobin level less than 120 g/L in males and 110 g/L in females).

12. Subject is malnourished by study physician's opinion

13. Subject has active cancers as self-report

14. Subject has lost or gained more than 5% of body weight in the past 3 months

15. Subject attends other clinical trials and is not approved by AN

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Peking Union Medical College Hospital Beijing
China Shanghai 6th People's Hospital Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Abbott Nutrition

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total skeletal muscle mass Dual X-ray Absorptiometry (DXA) Test Visit 1 (~ Day 13) No
Secondary Total body fat Test Visit 1 (~ Day 13) No
Secondary Total body fat free mass Test Visit 1 (~ Day 13) No
Secondary Total skeletal muscle mass Bioelectrical Impedance Absorptiometry (BIA) Test Visit 1 (~ Day 13) No
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