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

K

Kaohsiung Medical University

Status

Completed

Conditions

Hemolysis
Iron Deficiency
Inflammation
Sports Anemia
Oxidative Stress
Fatigue

Treatments

Dietary Supplement: Danggui Buxue Tang
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT02996786
MOST 106-2410-H-037-007-MY3

Details and patient eligibility

About

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

Full 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.

Enrollment

39 patients

Sex

Male

Ages

20 to 30 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

39 participants in 2 patient groups, including a placebo group

Danggui Buxue Tang group
Experimental group
Description:
Danggui Buxue Tang group receive orally supplementation of 7.5 g/day of Danggui Buxue Tang for 10 days
Treatment:
Dietary Supplement: Danggui Buxue Tang
Placebo group
Placebo Comparator group
Description:
Placebo group receive orally supplementation of 7.5 g/day of placebo for 10 days
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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