• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
Redalyc.Anisomycin Disrupts Consummatory Behavior after
Redalyc.Anisomycin Disrupts Consummatory Behavior after

... disruption, given that potential unspecific effects could not be attributed to anisomycin circulating in the rat’s system during Trials 11 or 12. As before, if anisomycin led to an erasure of Trial-11 memories, then the group thus treated should be delayed by one trial the onset of recovery from inc ...
Guideline Summary NGC-9333
Guideline Summary NGC-9333

... crossover period only was available, in which case the study could be analysed as a parallel trial. Placebo controlled trials were not included for the review question on the acute treatment of migraine as the GDG agreed that people seeking medical help for a migraine attack would have already tried ...
Striatal  D2 / D3  Receptor  Occupancy, ... and Side Effects with Amisulpride: An Iodine-123-Iodobenzamide SPET Study
Striatal D2 / D3 Receptor Occupancy, ... and Side Effects with Amisulpride: An Iodine-123-Iodobenzamide SPET Study

... males, 10 females) from the Department of Psychiatry at the University of Munich, who were suffering from schizophrenia (N = 26) or schizoaffective disorder (N = 3) (DSM IV). Their mean age was 31.7 years (31.7 ± 12.2 years, range: 19–68 years). All patients received continuous monotherapy with amis ...
OHR PHARMACEUTICAL, INC.
OHR PHARMACEUTICAL, INC.

... Notes to Unaudited Consolidated Financial Statements December 31, 2014 NOTE 1 – CONDENSED FINANCIAL STATEMENTS The accompanying consolidated financial statements have been prepared by the Company without audit. In the opinion of management, all adjustments (which include only normal recurring adjust ...
Full Report  - NIHR Journals Library
Full Report - NIHR Journals Library

... Second, the HTA programme provides grants for clinical trials for researchers who identify research questions. These are assessed for importance to patients and the NHS, and scientific rigour. Third, through its Technology Assessment Report (TAR) call-off contract, the HTA programme commissions besp ...
FDG-PET/CT - QIBA Wiki
FDG-PET/CT - QIBA Wiki

... that the test results may be valid within the context of the trial (see Sections 1.7.2, 3 and 4.2.2). Relative contraindications become absolute (i.e., Imaging Exclusion Criteria) when they cannot be remediated. When the FDG-PET/CT imaging endpoint is a trial endpoint, the subject would then be excl ...
Prozac - Eli Lilly and Company
Prozac - Eli Lilly and Company

... In controlled trials used to support the efficacy of fluoxetine, patients were administered morning doses ranging from 20 to 80 mg/day. Studies comparing fluoxetine 20, 40, and 60 mg/day to placebo indicate that 20 mg/day is sufficient to obtain a satisfactory response in Major Depressive Disorder i ...
NCIC CTG SC20 Protocol - Canadian Cancer Trials Group
NCIC CTG SC20 Protocol - Canadian Cancer Trials Group

... included in this study. The initial radiation dose to the extremities/ribs can be a single fraction of 6, 7 or 8 Gy, 18 Gy in 4 fractions, 20 Gy in 5 fractions, 24 Gy in 6 fractions, 27 Gy in 8 fractions or 30 Gy in 10 fractions. The initial radiation dose to metastases in the spine and pelvis can b ...
Vitamin B for treating peripheral neuropathy (Review)
Vitamin B for treating peripheral neuropathy (Review)

... The vitamin B complex functions as coenzymes in several intermediary metabolic pathways for energy generation and blood cell formation which cannot be explained simply. Thiamine is converted to thiamine pyrophosphate that functions in carbohydrate metabolism as a coenzyme in the decarboxylation of a ...
Stanislaw Burzynski, M.D., Ph.D. FDA Office of Prescription Drug
Stanislaw Burzynski, M.D., Ph.D. FDA Office of Prescription Drug

... Dr. V alladares is a Senior Oncologist at the Burzynski Clinic_ He g raduated Summa Cum Laude (First Place in his graduating class) from San Marcos University , Lima, Peru. He received an Award from the National A cademy of Medicine_ He w as Medical and Specialist Professor at University Hospital ev ...
Reporting of Harms Associated with Graded Exercise Therapy and
Reporting of Harms Associated with Graded Exercise Therapy and

... trembling/instability, insomnia, and sore throat/glands (64,65). These symptoms are not uncommon and can last days, if not weeks, for some individuals (65). In 2006, an audit of adult specialty ME/CFS rehabilitation (CBT/GET) clinics in Belgium (clinics that had been set up following a request from ...
Australian public assessment for vortioxetine hydrobromide
Australian public assessment for vortioxetine hydrobromide

... The TGA administers the Therapeutic Goods Act 1989 (the Act), applying a risk management approach designed to ensure therapeutic goods supplied in Australia meet acceptable standards of quality, safety and efficacy (performance), when necessary. ...
Ovarian cancer (stage I-IV) - Chemotherapy
Ovarian cancer (stage I-IV) - Chemotherapy

... chemotherapy for women with epithelial ovarian cancer. The level of evidence assigned to recommendations is based on the NHMRC Evidence Intervention Hierarchy (Appendix 1). Practice points are also provided to help guide clinical decisions for the use of first-line chemotherapy for women with epithe ...
Epclusa - Gilead
Epclusa - Gilead

... genotype 1, 2, 3, 4, 5, or 6 HCV, without cirrhosis or with compensated cirrhosis, who received EPCLUSA for 12 weeks. EPCLUSA was studied in placebo- and activecontrolled trials [see Clinical Studies (14.2)]. The proportion of subjects who permanently discontinued treatment due to adverse events was ...
Extract from Clinical Evaluation Report: Ivacaftor
Extract from Clinical Evaluation Report: Ivacaftor

... The Therapeutic Goods Administration (TGA) is part of the Australian Government Department of Health, and is responsible for regulating medicines and medical ...


... reagent. Their findings further suggest that for the paucibacillary type of samples, such as CSF, less sample reagent might be necessary. These findings need to be confirmed independently and should be combined with testing of the tuberculocidal effect at lower sample-to-sample-reagent ratios before ...
(PSD) November 2016 PBAC Meeting - (Word 109KB)
(PSD) November 2016 PBAC Meeting - (Word 109KB)

... The sponsor requested a hearing for this item. The clinician presented clinical case studies, including current clinical treatments for patients with this condition, how the drug would be used in current practice in Australia, and addressed other matters in response to the Committee’s questions. The ...
ZYRTEC-D 12 HOUR   (cetirizine hydrochloride 5 mg and
ZYRTEC-D 12 HOUR  (cetirizine hydrochloride 5 mg and

... intradermal injection of various other mediators or histamine releasers were also inhibited by cetirizine. In mildly asthmatic subjects, cetirizine at 5 to 20 mg blocked bronchoconstriction due to nebulized histamine, with virtually total blockade after a 20 mg dose. In trials conducted for up to 12 ...
Protocol - The EMMES Corporation
Protocol - The EMMES Corporation

... autologous transplants plus maintenance therapy versus the strategy of single autologous transplant plus consolidation therapy with lenalidomide, bortezomib and dexamethasone (RVD) followed by maintenance therapy or single autologous transplant plus maintenance therapy as part of upfront treatment o ...
Selegiline transdermal system in major depressive disorder
Selegiline transdermal system in major depressive disorder

... in the pool of short-term clinical trials was application-site reaction (STS: 24%; placebo: 12%). All of the application-site reactions were mild or moderate in severity and generally did not require further treatment such as topical steroids [101] . Table 2 summarizes all AEs reported by at least 2 ...
Policy for Procedures of Lower Clinical Value
Policy for Procedures of Lower Clinical Value

... Birmingham, Solihull and the Black Country into one common set. This helps us to stop variation in access to NHS services in different areas (which is sometimes called ‘postcode lottery’ in the media) and allow fair and equitable treatment for all local patients. CCGs have limited budgets; these are ...
English  - International Journal of Psychology and
English - International Journal of Psychology and

... disruption, given that potential unspecific effects could not be attributed to anisomycin circulating in the rat’s system during Trials 11 or 12. As before, if anisomycin led to an erasure of Trial-11 memories, then the group thus treated should be delayed by one trial the onset of recovery from inc ...
A Multi-Center, Randomized, Double Blind, Phase III Trial
A Multi-Center, Randomized, Double Blind, Phase III Trial

... primary endpoint will be GVHD free survival at Day 56 post randomization. Corticosteroids have been used as primary therapy for acute GVHD for many years. Historical published and unpublished data from Johns Hopkins, M. D. Anderson, University of Michigan and others defined an expected 35%-53% compl ...
2016 annual report - Ophthalmology and Visual Sciences
2016 annual report - Ophthalmology and Visual Sciences

... her estate to the Department in memory of her brother. This gift helped establish the Dr. John W. Doolittle Professorship of 1996. The Professorship was previously held by Burton Kushner, MD, Professor Emeritus, and former Pediatric Service Chief who was a mentor to Dr. Bradfield. The Doolittle Prof ...
Melanoma NCCN.org
Melanoma NCCN.org

... consult these guidelines is expected to use independent medical judgment in the context of individual clinical circumstances to determine any patient’s care or treatment. The National Comprehensive Cancer Network makes no representation or warranties of any kind regarding their content, use, or appl ...
< 1 ... 22 23 24 25 26 27 28 29 30 ... 170 >

Clinical trial

Clinical trials are experiments done in clinical research. Such prospective biomedical or behavioral research studies on human participants are designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietary choices, dietary supplements, and medical devices) and known interventions that warrant further study and comparison. Clinical trials generate data on safety and efficacy. They are conducted only after they have received health authority/ethics committee approval in the country where approval of the therapy is sought. These authorities are responsible for vetting the risk/benefit ratio of the trial - their approval does not mean that the therapy is 'safe' or effective, only that the trial may be conducted.Depending on product type and development stage, investigators initially enroll volunteers and/or patients into small pilot studies, and subsequently conduct progressively larger scale comparative studies. Clinical trials can vary in size and cost, and they can involve a single research center or multiple centers, in one country or in multiple countries. Clinical study design aims to ensure the scientific validity and reproducibility of the results.Trials can be quite costly, depending on a number of factors. The sponsor may be a governmental organization or a pharmaceutical, biotechnology or medical device company. Certain functions necessary to the trial, such as monitoring and lab work, may be managed by an outsourced partner, such as a contract research organization or a central laboratory.Only 10% of all drugs started in human clinical trials become an approved drug.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report