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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02996786
Other study ID # MOST 106-2410-H-037-007-MY3
Secondary ID
Status Completed
Phase N/A
First received December 11, 2016
Last updated April 18, 2018
Start date October 2016
Est. completion date July 2017

Study information

Verified date November 2016
Source Kaohsiung Medical University Chung-Ho Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to examine the beneficial effects of Danggui Buxue Tang on blood biochemical parameters in male recreational runners.


Description:

1. Male recreational runners would be recruited by community websites or email. After completely introducing the study, the participants would be requested to sign informed consent.

2. The participants would perform maximal oxygen consumption test prior to the supplementation. The participants would be supplemented with either Danggui Buxue Tang or placebo for a week before performing the 13-km run. A total of 4 times blood collection (before supplementation, immediate after running, 1 day and 3 days after running) would be performed for evaluating the effect of Danggui Buxue Tang on blood biochemical parameters.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria:

- The participants should have the experience finishing 10-km run but without the experience of attending a marathon run.

Exclusion Criteria:

- Participants suffering from anemia (Hb <13 g/dL), taking usual supplements, medication, alcohol or not feeling comfortable.

Study Design


Intervention

Dietary Supplement:
Danggui Buxue Tang
Danggui Buxue Tang purchased from Kaiser Pharmaceutical
Other:
Placebo
Consisting of corn starch and carboxymethyl cellulose

Locations

Country Name City State
Taiwan Kaohsiung Medical University Kaohsiung

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Medical University Chung-Ho Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hematological parameters Complete blood counts and serum haptoglobin and erythropoietin Through study completion, an average of 1 year
Primary Iron status Serum iron, ferritin, transferrin and hepcidin Through study completion, an average of 1 year
Primary Oxidative stress Thiobarbituric acid reactive substances, superoxide dismutase, catalase, and glutathione peroxidase Through study completion, an average of 1 year
Primary Inflammatory response High-sensitivity c-reactive protein, Tumor necrosis factor-alpha, and interleukin-6 Through study completion, an average of 1 year
Secondary Running time The completion time for a 13-km run Through study completion, an average of 1 year
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