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Methylphenidate for attention deficit hyperactivity disorder and drug relapse in
Methylphenidate for attention deficit hyperactivity disorder and drug relapse in

... method. Fisher’s exact test was calculated for the categorical variables. Retention in the trial, calculated up through the last visit at the clinic (or if the patient did not visit the clinic after the release, the day of release), was analysed using the Kaplan–Meier survival analysis. All statisti ...
The Effects of Nabilone on Sleep in Fibromyalgia: Results of a
The Effects of Nabilone on Sleep in Fibromyalgia: Results of a

... Cannabis has been reported by several patient populations to help sleep. We evaluated the safety and efficacy of nabilone, a synthetic cannabinoid, on sleep disturbance in fibromyalgia (FM), a disease characterized by widespread chronic pain and insomnia. METHODS: We conducted a randomized, double-b ...
Developing a consortium for ALS clinical research: the Canadian
Developing a consortium for ALS clinical research: the Canadian

... and expedite the requirements of pharmaceutical industry in preparing for clinical trials. The start process is streamlined whereby the study sponsors negotiate directly with CALS instead of contacting each individual site. A single confidentiality disclosure agreement can be signed by the CALS Chai ...
View CV - The Neurology Center of Southern California
View CV - The Neurology Center of Southern California

... A 6-month, Randomized, Active Comparator, Open-label, Multi- Center Study to Evaluate Patient OutComes, Safety and Tolerability of Fingolimod 0.5 mg/day in Patients with Relapsing Forms of Multiple Sclerosis who are candidates for MS therapy change from Previous Disease Modifying Therapy (EPOC).” – ...
July 17, 2007
July 17, 2007

... – Purpose: To compare the efficacy of 2mg and 4mg of E2007 and placebo on motor function – Treatment groups: 2mg, 4 mg or Placebo ...
Wesley Research Institute
Wesley Research Institute

... number of research projects carried out across three genre: ‘InvestigatorInitiated Research’, where the clinician devises an extensive project of major clinical relevance that is usually in collaboration with a scientist; ‘Patient Outcome/Clinical Improvement Research’, where the researchers are oft ...
Instructional Package - Horry Georgetown Technical College
Instructional Package - Horry Georgetown Technical College

... evaluations in one Learning Outcome, 3 unsatisfactory evaluations under different learning outcomes, or an incident of a critical event. A critical event is defined as, but not limited to: a dangerous action that injures or has the potential to injure, illegal or unethical behavior, and alcohol or d ...
Statistical Graphics and Reporting in Drug Development
Statistical Graphics and Reporting in Drug Development

... With current trends of diminishing drug pipelines, safety concerns and lengthy drug development processes, there is a critical need for efficiencies in drug development. The use of concise, compelling and standardized graphical analyses and reports can help create such efficiencies, while focusing a ...
Management of clozapine-resistant schizophrenia
Management of clozapine-resistant schizophrenia

... failure of maintenance and relapse despite seemingly adequate doses of antipsychotics. ...
Loratadine Prescribing Information.
Loratadine Prescribing Information.

... tap water can be used; however, as much as possible of the amount administered should be removed before the next instillation. Saline cathartics draw water into the bowel by osmosis and therefore may be valuable for their action in rapid dilution of bowel content. Loratadine is not removed by hemodi ...
Oral Disease-Modifying Therapies for Multiple Sclerosis
Oral Disease-Modifying Therapies for Multiple Sclerosis

... has progressed rapidly, affording physicians and patients broader options for disease management. Classical MS treatments using first-line injectable drugs, although widely applied, remain of major concern in terms of therapeutic adherence and efficacy. The IFNs, the first and (still) most commonly ...
Droxanol - nadurel pharma
Droxanol - nadurel pharma

... Devil’s  claw  (Harpagophytum  procumbens)   •  According  to  UpToDate  (www.uptodate.com):   –  "Devil's  claw  reportedly  improves  joint  mobility  and   reduces  pain  and  swelling  in  arthriIs."   –  "It  may  be  more  effecIve  for  ost ...
JRO Interventional Protocol Template
JRO Interventional Protocol Template

... Short title: Sponsor code: [Type sponsor protocol number] ...
Toxicology and safety pharmacology and metabolic studies
Toxicology and safety pharmacology and metabolic studies

... “Efficacy” (Proof of Concept), dose range, drug interactions, special patient populations (WoCBP, paeds) Phase III “Proving trials” double blind efficacy against disease target Phase IV Post marketing surveillance, Market Positioning ...
Sample slide presentation on Chelation Therapy
Sample slide presentation on Chelation Therapy

... Of the five clinical trials in which patients were randomly selected to receive chelation therapy or a placebo (a dummy solution), the most rigorous way of assessing a new treatment, three trials involved so few people that only a dramatic improvement could have been detected. Studies need larger nu ...
THE FIRST-AND-ONLY ONE DOSE IV treatment for flu
THE FIRST-AND-ONLY ONE DOSE IV treatment for flu

... In five randomized, double-blind, controlled trials, 1,399 subjects with acute uncomplicated influenza received a single dose of RAPIVAB, administered intravenously or intramuscularly, at doses up to 600 mg. Among the 664 subjects receiving RAPIVAB 600 mg (intravenous or intramuscular), the most com ...
Clinical Research Protocol
Clinical Research Protocol

... Even though subjects may be withdrawn prematurely from the study, it is imperative to collect at least survival data on such subjects throughout the protocol defined follow-up period for that subject (though careful thought should be give to the full data set that should to be collected on such subj ...
Spiriva Respimat [product monograph].
Spiriva Respimat [product monograph].

... Pregnant Women: There is a limited amount of data from the use of tiotropium in pregnant women. Animal studies do not indicate direct or indirect harmful effects with respect to reproductive toxicity (please refer to the Toxicology section of the Monograph). Because animal reproduction studies are n ...
Clinical Microbiology in the 21st Century
Clinical Microbiology in the 21st Century

... and specimens that are bacterial, viral, parasitological, or mycological (fungi) are sent to the clinical microbiology laboratory. Clinical microbiology laboratories provide services that are critical to the well-being of our population—analyzing specimens collected from sick patients and gathering ...
Topiramate in Migraine Prevention
Topiramate in Migraine Prevention

... Chronic migraine sufferers are already costing insurers a lot of money by the time they are referred for Botox treatment, and the additional costs are seen as marginal and the potential gains large. ...
JMP® versus JMP® Clinical for Interactive Visualization of Clinical Trials Data
JMP® versus JMP® Clinical for Interactive Visualization of Clinical Trials Data

... Both JMP and JMP Clinical can be used to produce interactive visualizations and analyses of clinical trials data. Those who have already adopted SDTM and/or ADaM can benefit from the pre-built workflows and dashboards of JMP Clinical. Reports on Findings, Interventions and Events domains are produce ...
What is clinical pharmaceutics?
What is clinical pharmaceutics?

... which can become trapped in diverticula in the gut, or injections that precipitate on administration. Most of the topics in this introductory chapter, aimed at introducing the field in a general way, will be discussed in more detail later in the book. ...
SIH
SIH

... Supervised injectable methadone maintenance – c 10k pppa ...
Anaphylaxis
Anaphylaxis

... Intubate if any indication of impending airway obstruction or angioedema. Remember with angioedema these may be difficult intubations. Be prepared for Cricothyrotomy. If normotensive can use standard RSI protocol. If hypotensive use ‘shock intubation’ protocol. ...


... The awakening question was designed to take into account the circadian variation of airway calibre in patients with asthma. Since bronchoconstriction occurs in the early morning hours (the nadir occurs near 06.00 h), the awakening question evaluates the entire overnight period, including symptoms th ...
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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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