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Clinical Expert Consensus Statement on Best Practices
Clinical Expert Consensus Statement on Best Practices

... update should reflect any changes in medical status (e.g., change in renal function) or medications that have occurred since the original H&P. For inpatients, an H&P should be performed within 24 hr of admission or registration, but prior to procedures requiring anesthesia services. At a minimum, th ...
DES - Minor Surgery
DES - Minor Surgery

... the need for removal (if required for diagnostic reasons removal will be performed by dermatologists, if not required for diagnostic purposes removal will not be performed by dermatologists)  Significant (future) risk of neoplasia  Lesions causing functional problems or significant disfigurement ( ...
headache and facial pain program
headache and facial pain program

... Migraine Classification. He has written over 400 original and review articles and six books including Wolff’s Headache and Headache in Clinical Practice. His papers defined the epidemiology and burden of migraine in the U.S. and lead to the development of widely used screening (ID Migraine) as well ...
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... separated from those of the family • When treatment is withdrawn, all efforts are to make baby comfortable – Sedatives that shorten life are OK – Killing the baby is not OK ...
1. THE IMPORTANCE OF ETHICS 1.1 Introduction South Africa is
1. THE IMPORTANCE OF ETHICS 1.1 Introduction South Africa is

... essential elements must be understood before a participant is capable of giving informed consent. ...
Part 2: Ethical Issues - Compassion and Support
Part 2: Ethical Issues - Compassion and Support

... discussion and resolution of conflicts. Basic nursing and comfort care (ie, oral hygiene, skin care, patient positioning, and measures to relieve pain and symptoms) must always be continued. DNAR orders carry no implications about other forms of treatment, and other aspects of the treatment plan sho ...
the alexander technique and the placebo effect
the alexander technique and the placebo effect

... But then some research studies showed that these drugs were no more effective than placebos. This caused doctors to lose confidence in them and the effectiveness of the drugs fell by half, down to 30-40 percent, which happened to be what the report of the trial described as the base-line placebo eff ...
Protocol - University of Colorado Denver
Protocol - University of Colorado Denver

... Co-morbid factors, including smoking, can further alter susceptibility for pneumonia in the setting of AUDs. For example, investigations in animal models have revealed that ciliary dysfunction is compounded in the presence of both alcohol and cigarette smoke compared to either exposure alone(15), su ...
Rapid acute treatment of agitation in individuals with schizophrenia
Rapid acute treatment of agitation in individuals with schizophrenia

... had been completed, and at least 12 h had elapsed after the last dose of the study drug, participants were discharged or stayed in the hospital depending on their clinical status and the judgement of the investigator. The study design was reviewed and approved by independent institutional review boa ...
Indian Journal of Anesthesia and Analgesia
Indian Journal of Anesthesia and Analgesia

... information that was available at the time the plan or protocol for the study was written such as study approach, design, type of sample, sample size, sampli ng te c hnique , se tting o f t he s tud y, description of data collection tools and methods; all information obtained during the conduct of t ...
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Respiratory Diseases - NATIONAL BOARD OF EXAMINATIONS

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Sample Policy for Organ Donation after Cardiac Death
Sample Policy for Organ Donation after Cardiac Death

... within their own hospitals for provision of ethical terminal care for organ donor patients and their families, with the assistance of guidelines developed by the Institute of Medicine and the United Network for Organ Sharing (UNOS). Anesthesiologists should be respectful of the wishes of donor patie ...


... received to bill for the device. Once IRB approval has been obtained, the Study Coordinator must contact Vidant Health Finance to complete the CMS packet. Vidant Health Finance will submit the packet to CMS and notify the Study Coordinator when approval for billing the device has been received. Once ...
PDF - Innovare Academic Sciences
PDF - Innovare Academic Sciences

... A clinical trial is a research study in human subjects with the aim of answering specific questions about a new medical treatment (vaccines, new therapies or new ways of using known treatments). Clinical trials (also called medical research and research studies) are used to determine whether new dru ...
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... 4. Research Coordinator/Assistant will indicate ID number from randomization system on order given to pharmacy 5. Pharmacy will match the ID number to the randomization list to determine allocated treatment ...
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The Urgent Need Regenerating antibacterial drug

... the IDSA 2004 Report Bad Bugs, No Drugs, which reports on sixteen new antibacterial agents being approved and brought to market between 1983-1987, compared with the estimate that between only two and four new antibacterial agents will reach market between 2008-2012. It is by no means clear if even t ...
Goran Vesov
Goran Vesov

... inconveniences should be weighed against the anticipated benefit for the individual trial subject and society. A trial should be initiated and continued only if the anticipated benefits justify the risks. 3. The rights, safety, and well-being of the trial subjects are the most important consideratio ...
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... • What is being compared to what? - two-arm trial: experimental intervention vs nothing, placebo - standard intervention, different dose or duration - multi-arm - factorial - groups ...
04 Nov 09 Research Fortnight Opportunities issue 334 Jeremy
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... These support short- and long-term focused projects and also broader-based programmes. Grants may last up to five years, but those of two years or less are for proof of principle or pilot work only. Funding at a rate of 80 per cent of full economic costs will be provided to cover a salary, consumabl ...
Approach to the Critique High Risk Clinical Trials
Approach to the Critique High Risk Clinical Trials

... Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this standard provides public assurance that the rights, safety and well-being of trial ...
ORIGINAL ARTICLE Morpho-anatomy of leaf, stem and root of
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... America1. In India, five species have been recorded, out of which Alternanthera sessilis (L.) R. Br. ex DC and Alternanthera pungens Kunth are utilized extensively as raw drug sources worldwide in many traditional systems of medicine.1,2 As drugs are collected by traditional practitioners who have i ...
Clinical Ethical Decision Making: The Four Topics Approach
Clinical Ethical Decision Making: The Four Topics Approach

... in a given case. Underlying this topic are the ethical principles of beneficence and nonmaleficence. Beneficence is what physicians aspire to do—to help patients by using their accumulated skills and knowledge in the promotion of healing, curing, and preventing risk. Nonmaleficence can be simply def ...
Clinical Ethical Decision Making: The Four Topics
Clinical Ethical Decision Making: The Four Topics

... in a given case. Underlying this topic are the ethical principles of beneficence and nonmaleficence. Beneficence is what physicians aspire to do—to help patients by using their accumulated skills and knowledge in the promotion of healing, curing, and preventing risk. Nonmaleficence can be simply def ...
N Innovations in Clinical Trial Design
N Innovations in Clinical Trial Design

... President of Clinical Research. Li and her team will work to expand NERI’s role as a private-sector CRO, while building on NERI’s 20-year reputation as a leading public-sector research organization. Reporting directly to NERI President, Sonja McKinlay, Li will manage clinical research operations and ...
the PDF
the PDF

... The Belmont Report identifies three fundamental ethical principles for all human subject’s research – respect for persons, beneficence, and justice. Those principles remain the basis for the HHS human subject’s protection regulations.  The Declaration of Helsinki: https://history.nih.gov/research/d ...
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Declaration of Helsinki

The Declaration of Helsinki is a set of ethical principles regarding human experimentation developed for the medical community by the World Medical Association (WMA). It is widely regarded as the cornerstone document on human research ethics.It is not a legally binding instrument under the international law, but instead draws its authority from the degree to which it has been codified in, or influenced, national or regional legislation and regulations. Its role was described by a Brazilian forum in 2000 in these words ""Even though the Declaration of Helsinki is the responsibility of the World Medical Association, the document should be considered the property of all humanity"".
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