oxidative stress injuries. -
Conditions
Interventions
Intervention 1: Intervention group:effervescent tablets of N-acetyl cysteine as 4 times starting 24 hours before the trial. Intervention 2: placebo group: dextrose %3 as dissolved in water.
Prevention
Placebo
Intervention group:effervescent tablets of N-acetyl cysteine as 4 times starting 24 hours before the trial
placebo group: dextrose %3 as dissolved in water
Sponsors
Deputy of Research,Bushehr University of Medical Sciences
Eligibility
Sex/Gender
All
Age
21 Years to 25 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: participants aged between 21 and 25; either sex; having Vo2 max between 35 to 40 ml/kg/min ; and living in the same dormitory ; all having the same type of food. Exclusion criteria: subjects who were consuming energetic drugs; smokers; those having any type of regular sport activity.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total antioxidant capacity. Timepoint: Before the consumption of drug; one hour before start of the exercise;Immidiately after exercise;after one at rest hour. Method of measurement: By ELISA method and commercial kits.;C-reactive protein (CRP). Timepoint: Before the consumption of drug; one hour before start of the exercise;Immidiately after exercise;after one at rest hour. Method of measurement: By ELISA method and commercial kits.;Malondealdehyde. Timepoint: Before the consumption of drug; one hour before start of the exercise;Immidiately after exercise;after one at rest hour. Method of measurement: By spectraphothometry. | — |
Secondary
| Measure | Time frame |
|---|---|
| BMI. Timepoint: Before the trial. Method of measurement: weight in kilograms divided by the square of height in meters.;Vo2 max. Timepoint: Before and after the trial. Method of measurement: Cooper Standard Aerobic Test was used. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Movahed
Bushehr University of Medical Sciences
Outcome results
None listed