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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03402308
Other study ID # 02-2017-010
Secondary ID
Status Completed
Phase N/A
First received January 10, 2018
Last updated April 13, 2018
Start date June 1, 2017
Est. completion date March 1, 2018

Study information

Verified date April 2018
Source Pusan National University Yangsan Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of the SCE on muscle strength, muscle mass, and muscle function in healthy adults for 12 weeks.


Description:

Previous studies have indicated that Schisandra chinensis extract (SCE) may have the ability to prevent skeletal muscle atrophy. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of the SCE on muscle strength, muscle mass, and muscle function in healthy adults; the safety of the compound are also evaluate. The Investigators examine the peak torque/body weight at 60°/s knee extension, handgrip strength, skeletal muscle mass, physical performance, and metabolic parameters at baseline, as well as after 4 and 12 weeks of intervention. Fifty-four healthy adults were administered either 1,000 mg of SCE or a placebo each day for 12 weeks;


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date March 1, 2018
Est. primary completion date March 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria:

- <110% of the standard lean body mass as measured using the body composition analyzer InBody 720)

- Body-mass index (BMI) ranging from 18.5 to 30.0 kg/m2

Exclusion Criteria:

- Abnormal liver or renal function (i.e., serum aminotransferase activity > 60 IU/L and serum creatinine concentrations > 1.2 mg/dL)

- Diabetes (diagnosed clinically or fasting glucose level > 126 mg/dL)

- History of fracture during the previous year

- Uncontrolled hypertension

- History of serious cardiac disease such as angina or myocardial infarction

- History of gastrectomy

- History of medication for psychiatric disease

- Administration of oriental medicine including herbs within the past 4 weeks

- Evidence of relatively high skeletal mass (more than 110% of the standard lean body mass as measured using the body composition analyzer InBody 720)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Schisandra chinensis extract
Schisandra chinensis extract 1,000 mg/day for 12 weeks
Placebo
Starch placebo 1,000 mg/day for 12 weeks

Locations

Country Name City State
Korea, Republic of Pusan National University Yangsan Hospital Pusan Ami-dong

Sponsors (1)

Lead Sponsor Collaborator
Pusan National University Yangsan Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary muscle strength the peak torque/body weight at 60°/s knee extension 12 weeks
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