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Effects of Danggui Buxue Tang on Blood Biochemical Parameters in Male Recreational Runners

Not Applicable
Completed
Conditions
Sports Anemia
Inflammation
Oxidative Stress
Hemolysis
Fatigue
Iron Deficiency
Interventions
Dietary Supplement: Danggui Buxue Tang
Other: Placebo
Registration Number
NCT02996786
Lead Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
Brief Summary

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

Detailed 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 & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
39
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Danggui Buxue Tang groupDanggui Buxue TangDanggui Buxue Tang group receive orally supplementation of 7.5 g/day of Danggui Buxue Tang for 10 days
Placebo groupPlaceboPlacebo group receive orally supplementation of 7.5 g/day of placebo for 10 days
Primary Outcome Measures
NameTimeMethod
Iron statusThrough study completion, an average of 1 year

Serum iron, ferritin, transferrin and hepcidin

Oxidative stressThrough study completion, an average of 1 year

Thiobarbituric acid reactive substances, superoxide dismutase, catalase, and glutathione peroxidase

Inflammatory responseThrough study completion, an average of 1 year

High-sensitivity c-reactive protein, Tumor necrosis factor-alpha, and interleukin-6

Hematological parametersThrough study completion, an average of 1 year

Complete blood counts and serum haptoglobin and erythropoietin

Secondary Outcome Measures
NameTimeMethod
Running timeThrough study completion, an average of 1 year

The completion time for a 13-km run

Trial Locations

Locations (1)

Kaohsiung Medical University

🇨🇳

Kaohsiung, Taiwan

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