healthy people
Conditions
Interventions
Three groups:administration arginine acetategranules
Sponsors
Daping Hospital, Third Military Medical University
Eligibility
Sex/Gender
Male
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. Body mass index(BMI) of 19 to 24 kg/m2 (inclusive); 2. No smoking, drinking or drug addiction before or during the study; 3. No history of cardiovascular, renal, gastrointestinal, hepatic, nervous, psychological disease or metabolic disorders.
Exclusion criteria
Exclusion criteria: 1. Subjects who took any over-the-counter or prescription drugs within two weeks or any arginine drug, food, health-care product, medicated diet within one week; 2. Subjects allergic to arginine; 3. Subjects who participated any investigational drug study within 1 months prior to this study; 4. Menstrual, pregnant or lactating women and women at childbearing age take oral contraceptive; 5. In the opinion of the investigator, subjects who are not suitable to participate in the study for whatever reasons must be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| concentrate of arginine acetate in plasma; | — |
Countries
China
Contacts
Public ContactXi Peng
Institute of Burn Research, Southwest Hospital, Third Military Medical University
Outcome results
None listed