Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
159 participants
INTERVENTIONAL
2015-05-31
2015-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effectiveness and Cost of a Quantitative and Qualitative Nutritional Supplementation in Elderly Patients
NCT00560729
Effectiveness Evaluation of Panax Ginseng, Vitamins and Minerals in Improvement of Stress and Fatigue
NCT01100632
A Specialized Nutraceutical for Pre-burnout
NCT04532892
Therapeutic Efficacy of Phytosterols on Metabolic Syndrome
NCT02969720
Fibersol-2 Clinical Trials Related to Appetite
NCT01305291
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Cistanche, is a desert plants in the family Orobanchaceae. It mainly grows in the sandy pastures of Inner Mongolia, Gansu and Xinjiang Province of China. The plants of the best quality is from Inner Mongolia. According to Traditional Chinese Medical theories, its nature and flavour is sweet, salty, warm, and goes into kidney, large intestine meridians. It is commonly used to invigorate the renal function, nourish essence and blood in the treatment of lumbar debility, impotence, infertility and muscles weakness, and regulates the intestinal tract environment such as dryness, and constipation. A clinical trial showed that Cistanche granules relieved kidney deficiency symptoms in 86.7% of the chronic fatigue syndrome patients, demonstrated a significant difference comparing post-intervention to baseline (P \<0.01).
Ginko As recorded in the Yuan Herbal Classic by Lulu Zhang Feng in Qing Dynasty, ginkgo has functions of reducing phlegm, detoxification, insect killing, could cure scabies and gangrene tumors, acute mastitis ulceration disease, dental caries, infantile diarrhea, leukorrhea with reddish discharge, chronic stranguria with turbid discharge, emission enuresis disease.
In addition, ginkgo can inhibit various types of pathogenic bacteria. A clinical study (conducted by Wuhan Military General Hospital) of over 100 subjects with high cholesterol showed that ginkgo extract (guanxin ketones) has antihypertensive effect.
Germany, United Kingdom, France, USA and South Korea also used ginkgo leaves to produce drugs for treating cardiovascular and cerebrovascular diseases.
Ginkgo root, containing ginkgo lactone C, M, A, B, is sweet, warm, plain and nontoxic, and can be used to treat leucorrhea disease and emission.
A study about late Alzheimer disease found that ginkgo can improve vascular patency, thus has notable effect in anti-aging of brain function in elderly people, and enhancing memories.
Subjects with ginkgo juice supplement showed significant improvement in memory, attention and complex movements compared to the control group, patients who take ginkgo juice have significantly improved.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Placebo
Placebo: Methyl cellulose and dextrose
Placebo Comparator: Placebo
Two tablets consume daily with meal.
Low dose
This blend contains Ginko at 120 mg/day and Cistanche at 300 mg/day
Experimental: Nutrilite® Low dose
Two tablets consume daily with meal.
High dose
This blend contains Ginko at 180 mg/day and Cistanche at 450 mg/day
Experimental: Nutrilite® High dose
Two tablets consume daily with meal.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Experimental: Nutrilite® Low dose
Two tablets consume daily with meal.
Experimental: Nutrilite® High dose
Two tablets consume daily with meal.
Placebo Comparator: Placebo
Two tablets consume daily with meal.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
memory loss or lack of concentration, muscle pain, sleep disturbances, continuous discomfort after labor; Or be diagnosed as CFS according to the clinical diagnosis 30-60 days before screening;
* Have normal electrocardiograms (ECG) and blood pressure during quiet respiration and during exercises.
* Be willing to use reliable contraception methods during the study period (only for volunteers with fertility).
* Agree not to take any medication, supplement or nutrition with promoting function to exercise capacity;
* Be willing to comply with all the requirements and procedures of the study;
* Agree to sign the informed consent form;
* Fully understand the nature, objective and the potential risks and side effects of the study.
Exclusion Criteria
* Female on menopausal;
* Have participated in similar clinical trials within 6 months before the screening;
* Currently taking medicines for cardiovascular or metabolic disease ;
* Have flu/symptoms of viral infection within three months before the first visit;
* Have history of or be diagnosed of any of the following diseases that may affect the study results: gastrointestinal disorders, hepatopathy, nephropathy, endocrine disease, blood disorders, respiratory and cardiovascular diseases;
* Current or previous alcohol abuser, currently taking or took illicit drugs, substance or over the counter prescription drugs which promote athletic performance;
* Subject with iron-deficiency anemia, diabetes mellitus, epilepsy, bleeding tendency or Coagulation disorders;
* Currently suffering from any gastrointestinal disorders or skeletal muscle dysfunction, including but not limited to: irritable bowel syndrome, colitis, ulcerative colitis, celiac disease, osteoporosis or arthritis;
* Currently having or had any medical or nutritious therapies, including taking protein supplements or nutrients that promote exercise capacity within 3 months before screening;
* Have lost or gained weight over 5 kilograms within 3 months before screening;
* Had hospitalizations within 3 months before screening;
* According to investigator's judgement, current frequent users of drugs which may affect the electrolyte balance or hydration.
* Pregnant or nursing female, as determined by a questionnaire.
35 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sinphar Pharmaceutical Co., Ltd
OTHER
Sprim Advanced Life Sciences
OTHER
Fudan University
OTHER
Access Business Group
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Shuguang Li, PhD
Role: PRINCIPAL_INVESTIGATOR
Fudan University, Department of Nutrition and Food Hygiene
References
Explore related publications, articles, or registry entries linked to this study.
1. Li Y, He DJ, Jiang ZL, Wu YQ and al. Studies on Emotional characteristics of individuals with chronic fatigue syndrome. China Journal of rehabilitation medicine, 2006, 21(3):218-220
2. Zhang J. Clinical study on behavior intervention in chronic fatigue syndrome. Liaoning Journal of Traditional Chinese Medicine, 2009, 36(8):1338-1340.
Fukuda K, Straus SE, Hickie I, Sharpe MC, Dobbins JG, Komaroff A. The chronic fatigue syndrome: a comprehensive approach to its definition and study. International Chronic Fatigue Syndrome Study Group. Ann Intern Med. 1994 Dec 15;121(12):953-9. doi: 10.7326/0003-4819-121-12-199412150-00009.
4. Shen XH, Zheng L, Zhu WR, Xu JZ, Chen JX and al. Clinical effect observation of Cistanch Yishen granule in the treatment of kidney deficiency type of chronic fatigue syndrome. China Pharmacy, 2008, 19(18):1416-1418.
5. Jean Carper.Magical Food.Beijing: Xinhua Publishing
Dou GX. Diet Guide, 1981, Jiangsu Sci and Tech Publishing.
Kan J, Cheng J, Hu C, Chen L, Liu S, Venzon D, Murray M, Li S, Du J. A Botanical Product Containing Cistanche and Ginkgo Extracts Potentially Improves Chronic Fatigue Syndrome Symptoms in Adults: A Randomized, Double-Blind, and Placebo-Controlled Study. Front Nutr. 2021 Nov 26;8:658630. doi: 10.3389/fnut.2021.658630. eCollection 2021.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13-SC-4-STL-002
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.