botanical profiles product and clinical trial information

... insignificant or irrelevant Dosage and duration of use Daily Dose in Clinical Trials: The doses used in the clinical trials and reported in the Table of Clinical Trials in the full monograph use ... in Clinical Trials: The doses used in the clinical trials and reported in the Table of Clinical Trials (below) use the manufacturer’s recommended dose All of the studies use the European products, ... pharmacology and toxicology Among her publications she has authored over 300 reviews and summaries of clinical trials and systematic reviews for the American Botanical Council’s HerbClip service and Research...

Ngày tải lên: 17/03/2014, 17:20

... analyses, and protocol amendments Full clinical trial reports were not available for eight trials, but extensive clinical trial summaries were provided Information was extracted directly from the clinical ... Clinical ulcers and bleeds Clinical ulcers and bleeds in the company clinical trial reports were as reported by investigators, and were not subjected to independent, blinded adjudication in trials ... arthritis was conducted using information from company clinical trial reports, supplied by Pfizer Ltd, of completed randomised, double-blind trials from the celecoxib clinical trials programme The objectives...

Ngày tải lên: 09/08/2014, 06:22

Ngày tải lên: 09/08/2014, 07:20

... in both medical and surgical patients [12] Therefore, we conducted a randomised clinical trial to assess the efficacy and safety of intensive insulin therapy compared with standard glucose control ... Substitution and Insulin Therapy in Severe Sepsis trial, a randomised multicentre trial designed to assess the efficacy and safety of intensive insulin therapy in patients with severe sepsis and septic ... involved in the treatment and investigation were unaware of the randomised schedule and the block size Interventions Patients were randomly assigned to receive either standard insulin therapy or...

Ngày tải lên: 25/10/2012, 10:35

... The present clinical trial evaluated the safety and efficacy of UC-II in the treatment of the knee in OA patients Materials and Methods Study Design This clinical trial (Human Clinical Trial Approval ... use, and product compliance Visit Visit Visit Visit Randomization Clinical assessments as indicated; first dose in clinic Clinical assessments as indicated Clinical assessments as indicated Clinical ... efficacy and safety assessments used in this study were standard for OA and are widely used and recognized as reliable, accurate, and relevant WOMAC scores were determined, at screening, and baseline,...

Ngày tải lên: 26/10/2012, 09:48

... readily capable of providing the date and time of access and the user name, and in many cases can also provide information about what information was accessed and the user’s action (such as create, ... as electronic health information exchange expands and standards for such exchange are adopted, we intend to work with ONC to assess whether such standards should include information about the ... access and amend protected health information at §§ 164.524 and 164.526, which are both limited to protected health information about an individual in a designated record set We believe that this information, ...

Ngày tải lên: 06/03/2014, 15:20

... Brocades and the Standing-Style Eight-Section Brocades From a clinical point of view, it means that it can be practiced by Int J Geriatr Psychiatry 2003; 18: 441–449 443 a clinical trial on ... Regulate Spleen and Stomach Participants Look Back to Treat Five Strains and Seven Impairments Sway Head and Buttocks to Expel Heart-Fire Pull Toes with Both Hands to Reinforce Kidney and Waist Clench ... Clench Fists and Look with Eyes Wide Open to Build up Strength and Stamina Rise and Fall on Tiptoes to Dispel All Diseases Qigong is a complete exercise for both the body and the mind Li and Sun (1997)...

Ngày tải lên: 28/03/2014, 19:21

... procedures and also summarized the patient information for the manuscript RK designed research, analyzed data and wrote the paper He initiated and designed the study and wrote the clinical protocol ... Her2 before and after Her2-pDNA vaccination A-D Her2-specific IFN-g production by T-cells from patients #3, 4, and 8, before (3 days pre-) and after (10 days post-) Her2-pDNA vaccination and at long ... a CD8+ T-cell response and protection from tumor challenge in conventional and human Her2-transgenic BALB/c and HLA-A2 transgenic B6 mice [25,38] The present clinical trial is the first to combine...

Ngày tải lên: 18/06/2014, 16:20

... acquiring clinical and laboratory data, data analysis and interpretation, and drafted the manuscript PP and LG participated in acquiring clinical and laboratory data, data analysis and data interpretation ... interpretation and drafted the manuscript LG, JV, and SQ participated in acquiring clinical samples and follow-up clinical information MSC participated in study design and coordination, data analysis and ... stratification and clinical outcome prognosis Page of 11 with local disease (stage I to resectable stage III) were treated surgically and those with advanced disease (stage III and IV) received systemic and/ or...

Ngày tải lên: 18/06/2014, 16:20

... (ICH)-Good Clinical Practice (GCP)-registered phase I/II clinical trial of rh-HGF As this application is the first clinical trial to administer rh-HGF to humans, we performed additional preclinical ... jaundice, and urinary findings, including proteinuria and microhematuria, caused by bladder catheter Platelet count and serum albumin level decreased to 6.9 × 104/ μL, and 3.2 g/dL, respectively, and ... the HGF-FH Clinical Study Team including Ms Harue Tada, Ms Akiko Matsuyama, Ms Ikuyo Bando, Ms Tomoko Yokota, Ms Kazumi Miura, and Mr Tatsuya Ito for implementation of the clinical trial; Dr Hajime...

Ngày tải lên: 18/06/2014, 19:20

... Health and Quality of Life Outcomes 2008, 6:113 Background Sleep is an important element of functioning and wellbeing and is associated with clinical status and general health Indeed, ... Germany, Hungary, Poland, Australia, the United Kingdom and South Africa were screened for the clinical trial Selected patients had to have been diagnosed with type I or II diabetes and with painful, ... Effect Size (ES) and the Standardized Response Mean (SRM) were calculated, with the following values used for the interpretation of ES and SRM: ES and SRM = 0.20, small change; ES and SRM = 0.50,...

Ngày tải lên: 18/06/2014, 19:20

... admission or discharge and symptom or function scores Patients who qualified for the open-label extension of the three randomized clinical trials and who had usable scale scores and valid hospitalization ... (not including nicotine and caffeine addiction) Additional inclusion and exclusion criteria are presented in the previous reports from the randomized blinded phase of these trials [17-20] Patients ... symptomatology (≥ 75 and < 95), and low symptomatology (< 75) patient groups, respectively These cut-off points have been used in previous studies, and they also correspond to points slightly below and Page...

Ngày tải lên: 08/08/2014, 23:21

... treatment-resistant unipolar depression is supported by only a single randomized clinical trial [9] While it may be argued that many Diagnostic and Statistical Manual for Mental Disorders, fourth edition ... evaluation time) and week 24 (endpoint) along with repeated medical monitoring including ECG recording Patients could leave the study at any time and still obtain clinical care Study procedures and efficacy ... examinations MB, GR, AE and SC helped in retrieving literature references and/ or in patient enrollment and follow-up GP served as senior study consultant All authors read and approved the final...

Ngày tải lên: 09/08/2014, 01:21

... of SSc patients and controls to determine whether SSc patient have differences in plasma cytokines and whether these profiles correlate with autoantibody subsets of SSc Materials and methods Systemic ... and methods Systemic sclerosis patients and controls Patients and unrelated controls were selected from the Scleroderma Family Registry and DNA Repository and University of Texas Rheumatology Division, ... levels of IL-17 (P = 0.0009) and IL-23 (P = 0.04) No differences were observed in circulating levels of IL-1β, IL-2, IL-4, IL-5, IL8, IL-10, and IFNγ Table Demographics and clinical data of the cohort...

Ngày tải lên: 09/08/2014, 14:22

... television, kitchen, and private shower and bathroom facilities Volunteers were provided with food of their own choosing (except for alcohol and caffeine) and were free to prepare and eat food ad ... home and 349 lux, 381 lux, and 30 lux respectively for treatments A, B, and C in the laboratory However, the acrophases of 24hour Actillume illumination measured in lux were 13:09 at home and ... Table 1: aMT6s acrophase and measures of circadian malsynchronization and phase dispersion in older (n = 60, ages 60–79) and young volunteers (n = 30, ages 20–40), mean and SE Age Group Baseline...

Ngày tải lên: 10/08/2014, 09:20

... coagulation-fibrinolysis parameters and interpretation JMB and BM, was responsible for determination of IL-6 and interpretation RM was the surgical team and was responsible for preoperative clinical and analytical ... interpretation, and drafting the manuscript MB, LL, RP and MLM, were responsible for data collection and processing blood simples during the study and provided useful suggestions PM and JMR, was ... means between groups in clinical signs (bleeding) and laboratory parameters (D-dimer, creatine kinase and troponin I) at baseline, h and 24 h after surgery For bleeding and D-dimer, correction...

Ngày tải lên: 10/08/2014, 09:22

... requirements and design We then summarize the issues of overlapping functionality between BDMS and CRIS software, and user interfaces to clinical/ biospecimen data 2.1 Workflow of Biospecimen Collection and ... aliquot containers (vials) and the barcode labels record standard information such as patient ID, event, sample type and aliquot number The samples are batch shipped and aliquots that are received ... Status and Future Directions While TrialDB has been in production use at Yale and elsewhere for at least a decade, the integrated BDMS functionality has been implemented relatively recently, and...

Ngày tải lên: 10/08/2014, 09:22

... rural alberta clinical trial in optimizing hypertension (Rural RxACTION): trial design and methods Implementation Science 2011 6:94 Submit your next manuscript to BioMed Central and take full ... Setting Sample size and statistical analysis Pharmacists and pharmacies are selected based on their current practice model, size, and location of the community (population of < 20,000 and located more ... hypertension and blood pressure [25], as well as patients’ level of understanding and experience with pharmacy interventions [27,28] We plan to compare hypertension knowledge at baseline and at follow-up...

Ngày tải lên: 10/08/2014, 11:20

... and grade III ranged from 19% to 59% and 41% to 81% respectively across the three trials Figure displays the ratios of grade II to grade III tumors grouped by trial (a) and pathologist (b), and ... 8a-d) Association between outcome and clinical variables For each trial, outcome analyses were undertaken using clinical and pathological data The following clinical variables were considered: ... collection and data analysis, and drafted the manuscript MK and JB contributed to data analysis DF-B, FG, CG, and TP contributed to study design and undertook pathology review DF, MM, JG, and RG...

Ngày tải lên: 11/08/2014, 07:21