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Clinical Guidelines Handbook for Nurse Anesthesia
Clinical Guidelines Handbook for Nurse Anesthesia

... The Clinical Guidelines Handbook is intended to be used in conjunction with other University documents such as the University of Arizona Graduate Catalog and the DNP Program Handbook. Students should first consult the appropriate Program Handbook from the College of Nursing, the Clinical Guidelines ...
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

... Patol Kashaya is the decoction made with boiling cleaned, dried & yavkut [Nimbapatra(Azadirecta indica) & Patolpatra(Trichosanthes diocea)]11,12 in 16 times of water till water remaines 1/8th 13. While various researches have been made in the field of Medical Science, but still there is no absolute, ...
Emtriva - Gilead Sciences, Inc.
Emtriva - Gilead Sciences, Inc.

... should be exercised when administering nucleoside analogs to any patient with known risk factors for liver diseases; however, cases have also been reported in patients with no known risk factors. Treatment with EMTRIVA should be suspended in any patient who develops clinical or laboratory findings s ...
Treatment for sialorrhea (excessive saliva) in people with
Treatment for sialorrhea (excessive saliva) in people with

... An extensive search of the literature identified only one randomized controlled trial, of 20 patients, which could be included in the review. This study reported a beneficial effect of botulinum toxin type B injected into the parotid and submandibular salivary glands in patients with MND on a single ...
protocol - Tumori Rari Piemonte
protocol - Tumori Rari Piemonte

... Furthermore, RECIST responses and non dimensional responses clearly showed that the study drug objectively halted tumor progression. Notwithstanding, sorafenib caused responses lasting more than six months in only few patients and no response at all in almost 50% of Osteosarcoma patients. Under this ...
Institutional Resources/Facilities Pages
Institutional Resources/Facilities Pages

... The NPP includes over a dozen faculty members and staff who are experts in their fields and are able to provide multi-disciplinary feedback in areas relevant to clinical and translational research including, but not limited to, epidemiology, exercise medicine, biostatistics, health economics, health ...
Read a PDF of the entire series.
Read a PDF of the entire series.

... early preclinical studies that have since been identified, Grimm told Alzforum. It used large groups of up to 24 mice in each experiment, was blinded, and saw the same effect by way of different routes of administration in different mouse strains, whose transgene copy number was confirmed for each s ...
Alcobra Corporate Presentation November 2014 NASDAQ: ADHD
Alcobra Corporate Presentation November 2014 NASDAQ: ADHD

... This presentation includes statements that are, or may be deemed, ‘‘forward-looking statements.’’ In some cases, these forward-looking statements can be identified by the use of forward-looking terminology, including the terms “believes,” “estimates,” “anticipates,” “expects,” “plans,” “intends,” “m ...
Good practice guide for clinical radiologists Second edition
Good practice guide for clinical radiologists Second edition

... and public expectation. This best practice guidance is an essential resource to help you in this process and describes what are your individual responsibilities as well as those of the organisation in which you work. These good practice guidelines are clearly set out with useful links to more detail ...
gamunex - Grifols Canada
gamunex - Grifols Canada

... distress, pulmonary edema, hypoxemia, normal left ventricular function, and fever and typically occurs within 1-6 hrs after transfusion. Patients with TRALI may be managed using oxygen therapy with adequate ventilatory support. IGIV recipients should be monitored for pulmonary adverse reactions. If ...
Antiobesity Pharmacotherapy for Patients with Type 2 Diabetes
Antiobesity Pharmacotherapy for Patients with Type 2 Diabetes

... Modification and Lorcaserin Second Study for Obesity Management (BLOSSOM), and BLOOM-diabetes mellitus (BLOOMDM) [21-23]. The BLOOM and BLOSSOM trials investigated the effect of lorcaserin on overweight or obese nondiabetic patients and found a ~3% placebo-corrected weight change in the group treate ...
Fentanyl citrate - Therapeutic Goods Administration
Fentanyl citrate - Therapeutic Goods Administration

... dogs ~10 min compared with rats ~30-50 min) and linear relative to dose. Both oral and sublingual bioavailability was substantially higher in dogs than in rats, appearing to be complete for sublingual administration (>95%) and even appearing to be in excess of IV exposure at the highest tested dose ...
Prevalence and predictors of potential drug
Prevalence and predictors of potential drug

... Knowledge about exposure of population to clinical significant DDIs as well as the knowledge about risk factors for DDIs are the basis for taking measures to their management. For that purpose, the prevalence of potential DDIs was examined. Results presented that risk for DDIs varied widely, ranged ...
!  Topical timolol treatment for infantile hemangiomas: a phase II
! Topical timolol treatment for infantile hemangiomas: a phase II

... Anogenital IHs are often complicated by ulceration and infection, and affected infants often experience painful urination and defecation (1). IHs affect mostly the head and neck, which are visible locations. Craniofacial disfigurement in general has long been recognized as associated with negative p ...
Course Title - Stephen F. Austin State University
Course Title - Stephen F. Austin State University

... members promote academic integrity in multiple ways including instruction on the components of academic honesty, as well as abiding by university policy on penalties for cheating and plagiarism. Definition of Academic Dishonesty Academic dishonesty includes both cheating and plagiarism. Cheating inc ...
Towards comprehensive syntactic and semantic annotations of the
Towards comprehensive syntactic and semantic annotations of the

... systems to perform the same annotations automatically. Our effort focuses on developing principled and generalizable enabling computational technologies and addresses the urgent need for annotated clinical narratives necessary to improve the accuracy of tools for extracting comprehensive clinical in ...
PL 08081/0050-2 - Medicines and Healthcare products Regulatory
PL 08081/0050-2 - Medicines and Healthcare products Regulatory

... For information about side effects that may occur with using Elvanse 30, 50 and 70mg capsules, please refer to the PIL or the Summary of Product Characteristics (SmPC) available on the Medicines and Healthcare products Regulatory Agency (MHRA) website. Why are Elvanse 30, 50 and 70mg capsules approv ...
The PCORI Methodology Report PCORI Methodology Committee  Editors
The PCORI Methodology Report PCORI Methodology Committee Editors

... Initial topics were chosen to reflect areas where there were either substantial deficiencies or inconsistencies in how available methods were applied in practice or where there was specialized knowledge in how best to conduct research or to surmount barriers to the effective dissemination of researc ...
DAY 1 - American College of Physicians
DAY 1 - American College of Physicians

... skin biopsy with pathology returning for malignant melanoma. CT guided biopsy of intraabdominal mass was then obtained which showed poorly differentiated malignancy, suspicious for melanoma. Treatment: At the time of diagnosis, patient was inpatient in the Huntsman Cancer Hospital for pain control a ...
Starr Study Protocol - NDM Research Building
Starr Study Protocol - NDM Research Building

... 3.1. Current treatment strategies using corticosteroids and antibiotics The clinical response to treatment varies considerably and is associated with significant side effects. Our current inability to target therapy means some patients are inappropriately treated placing a vulnerable population at f ...
Salmeterol/Fluticasone STADA 25 μg/50 μg/dose, 25 μg/125 μg
Salmeterol/Fluticasone STADA 25 μg/50 μg/dose, 25 μg/125 μg

... medicinal product, which is legally allowed once the data protection time of the dossier of the reference product has expired. For this kind of application, it has to be demonstrated that the pharmacokinetic/ pharmacodynamic profile of the product is similar to the pharmacokinetic/pharmacodynamic pr ...
New Oral Anticoagulants in Atrial Fibrillation and Acute Coronary
New Oral Anticoagulants in Atrial Fibrillation and Acute Coronary

... patients 75 to 80 years of age, a dose reduction to 220 mg taken as one 110-mg capsule twice daily should be considered. The lower dose is mandatory for patients older than 80 years of age. No dose adjustment is needed with concomitant use of the P-glycoprotein (P-gp) inhibitor amiodarone, but in pa ...
July
July

... trial will be powered to detect an increase in RFS rate by 6.8% at 2 years, by 9.4% at 5 years, and by 10% at 10 years. The trial will be powered to detect a hazard ratio of 0.7 for overall survival. The trial design and statistical analysis plan must adequately address the comments provided to you ...
Product Monograph
Product Monograph

... impairment (CrCl30 mL/min) or on dialysis as these patients were excluded from pivotal Phase III trials. Therefore, LIXIANA is not recommended in these patients. Patients who develop acute renal failure while on LIXIANA should discontinue such treatment (see DOSAGE AND ADMINISTRATION and ACTION AND ...
1.3 Guidance Notes - Introduction
1.3 Guidance Notes - Introduction

... The provision of electronic solutions to support this increased clinical information document sharing relies on effective, efficient and consistent indexing naming, filing and metadata tagging of the same kinds of documents across all NHS boards sharing partners (which may be all boards). In recent ...
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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.
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