Status:
UNKNOWN
Study for Effectiveness Evaluation of Panax Ginseng, Vitamins and Minerals (Natugerin®) in Improvement of Stress and Fatigue
Lead Sponsor:
Azidus Brasil
Conditions:
Stress
Fatigue
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
It is hoped that the group treated with Panax Ginseng, Vitamins and Minerals obtain significant reduction in levels of stress and fatigue and that the results are superior to the placebo group.
Eligibility Criteria
Inclusion
- Agree with all study procedures, signing the IC in two ways, by his own free will;
- Patients older than 18 years, male or female, regardless of ethnicity or social class;
- Presence of pictures of mild to moderate stress, confirmed with the aid of the Stress Symptom Inventory (ISS), which considers stress and mild to moderate classification Alert classification Resistance;
- Presence frame of fatigue with a score greater than 36 according to the Fatigue Severity Scale (FSS).
Exclusion
- Participation in clinical trials in the 12 months preceding the survey;
- Current treatment with drugs that are stimulants or central nervous system depressants such as hypnotics, anxiolytics, antipsychotics, antidepressants, statins and muscle relaxants;
- Alternative Therapies that scientifically, or have no influence in the tables of stress or fatigue as acupuncture or relaxing massages;
- Treatment psychotherapeutic medication or not;
- Current treatment or prediction of treatment with oral anticoagulants (due to interaction with the tocopherol);
- Women who are pregnant or lactating;
- Patients with lactose intolerance;
- Patients allergic to soy or peanuts;
- chronic renal failure;
- Patients using other multivitamins or individual vitamins such as vitamin D and / or A.
- Chronic alcoholism;
- Patients with clinical diagnosis of diseases causing severe chronic pain or adversely affect the clinical interpretation as fibromyalgia, multiple sclerosis, neuropathies and myopathies;
- Patients with hypothyroidism or hyperthyreosis diagnosed clinically;
- Patient history and physical examination suggestive of severe hepatorenal failure;
- Patients with decompensated diabetes mellitus (fasting glucose above 180 mg / dL);
- Patients being treated for cancer;
- Amendment of the routine of life during the study as early vacation or suspected change in working hours;
- Patients with complaints of excessive sleepiness caused by organic source frameworks such as sleep apnea and morbid obesity (BMI above 35);
- History of hypersensitivity to any component of the product under investigation;
- Any finding of clinical observation (clinical history or physical examination) that is interpreted by the physician investigator as a risk to the patient's participation in the study.
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2011
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT01228006
Start Date
September 1 2011
End Date
December 1 2011
Last Update
October 25 2010
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