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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04742244
Other study ID # 00002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 28, 2020
Est. completion date August 13, 2020

Study information

Verified date March 2021
Source National Taiwan Sport University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the present study, investigators investigated whether supplementation with lemon verbena extract (LVE) could improve muscle damage and biochemical indicators after exhaustive exercise challenge. Based on maximum jump heights, 60 subjects (30 males and 30 females) were equally divided into a placebo group (0 mg/human/day) and an LVE supplement group (400 mg/human/day), with gender-equal distribution. All subjects started supplementation 10 days before exhaustive exercise and continued it until all tests were completed. Before the intervention, after the exhaustive exercise, and on the following 3 days, the participants underwent 12-minute Cooper running/walking; blood collection; assessments of pain, muscle stiffness, maximum jump heights, and isometric maximum muscle strength; and anaerobic strength tests.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 13, 2020
Est. primary completion date July 28, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria: - health - Must be able to swallow tablets Exclusion Criteria: - non-smokers - no musculoskeletal - medical - metabolic disease - women not on the reproductive cycle - high blood pressure, asthma - skeletal neuromuscular injuries in the upper or lower extremities

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Lvemon verbena extract
Each capsule contained 200 mg of lemon verbena extract 2 capsules/day, 14 days
maltodextrin
Each capsule contained 0 mg of lemon verbena extract 2 capsules/day, 14 days

Locations

Country Name City State
Taiwan National Taiwan Sport University Taoyuan

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan Sport University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary inflammation of IL-6 level To assess inflammation indicators, volunteers fasted for at least 8 hours before performing muscle exhaustion exercises. At designated time points in the recovery period, including baseline (0) and 3h, 24h, and 48 after exercise, blood samples were collected with brachial venous catheters. Assess serum IL-6 levels (pg/ml) to monitor physiological fitness. Used commercial kit human IL-6 immunoassay (R&D system, Minnesota, USA) and Elisa reader (PerkinElmer, Massachusetts, USA) for analysis 10 days
Primary Clinical Biochemistry of CK level To assess muscle damage, volunteers fasted for at least 8 hours before performing muscle exhaustion exercises. At designated time points in the recovery period, including baseline (0) and 3h, 24h, and 48 after exercise, blood samples were collected with brachial venous catheters. Serum CK (U/L), were assessed for monitoring physiological adaptation. All biochemical indices were assessed using an autoanalyzer (Hitachi 7060, Tokyo, Japan). 10 days
Primary Stress hormones 8-Hydroxy-2'-Deoxyguanosine (8-OHdG) in Urine Subjects' urine was collected 24 hours after the exhaustive exercise for analysis. Used commercial kit human 8-OHdG (Cayman, Mich, USA) and Elisa reader (PerkinElmer, Massachusetts, USA) for analysis 10 days
Primary Assessment of muscle stiffness 3 h, 24h, 48h after exhausting exercise, use Myoton machine to evaluate muscle stiffness (N/m) (Myoton, Tallinn, Estonia) 10 days
Primary Visual Analogue Scale (VAS) evaluation 3 h, 24h, 48h after exhausting exercise, use VAS questionnaire to record muscle pain. the minimum is 0 and maximum is 10, and whether higher scores mean more pain 10 days
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