Skip to content

Study on the Antiaging Effect of Chinese Herb Drink

Study on the Antiaging Effect of Chinese Herb Drink

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02634242
Enrollment
60
Registered
2015-12-18
Start date
2008-04-30
Completion date
2009-04-30
Last updated
2015-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecological Disorders

Keywords

Si Wu Tang, antioxidation, anthropometric measurements, liver, skin

Brief summary

The purpose of the current study was to check the physiological improvement of SWT on liver and skin and also the antioxidation in healthy adults.

Detailed description

Background: Si-Wu-Tang (SWT) is a well-known traditional Chinese medicine (TCM) and widely used for treating various gynecological disorders. The purpose of the current study was to check the physiological improvement of SWT on liver and skin and also the antioxidation in healthy adults. Methods: Sixty healthy voluntary subjects were recruited and assigned into two groups, who drank 125 mL of placebo (n=30) or SWT (n=30) for 6 continuous days per month during the following 6 months and vice versa with one month of washout period in between. During the initial, 3rd, 6th, 10th, and 13th months anthropometric measurements were performed as well as fasting blood samples were drawn for various biochemical assays. Abdominal ultrasonic and skin examination were performed at the initial, 6th and 13th months.

Interventions

OTHERSi-Wu-Tang (SWT)

The purpose of the current study was to check the physiological improvement of SWT on liver and skin and also the antioxidation in healthy adults.

OTHERplacebo

The purpose of the current study was to check the physiological improvement of placebo on liver and skin and also the antioxidation in healthy adults.

Sponsors

Chung Shan Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy adults

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frame
Total thiobarbituric acid reactive substances (TBARS)6 months

Secondary

MeasureTime frame
Total antioxidant capacity (TEAC)activities.6 months
Superoxide dismutase (SOD) activity6 months
GPx and glutathione reductase (GR) activity6 months
Catalase6 months
Glutamic oxaloacetic transaminase (GOT)6 months
Glutamic pyruvic transaminase (GPT)6 months
Glutathione content (GSH)6 months

Other

MeasureTime frame
Skin surface water loss6 months
Skin melanin index6 months
Skin elasticity6 months
Skin hydration6 months
Skin sebum content6 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026