LAKEWOOD, N.J. — November 13, 2015 — The results of a randomized control
trial study conducted by Magnolia Consulting, an independent evaluation consulting firm, has confirmed that Achieve3000's programs are extremely effective at improving students» literacy skills.
Not exact matches
Actual results and the timing of events could differ materially from those anticipated in the forward - looking statements due to these risks and uncertainties as well as other factors, which include, without limitation: the uncertain timing of, and risks relating to, the executive search process; risks related to the potential failure of eptinezumab to demonstrate safety and efficacy in clinical testing; Alder's ability to
conduct clinical
trials and
studies of eptinezumab sufficient to achieve a positive completion; the availability of data at the expected times; the clinical, therapeutic and commercial value of eptinezumab; risks and uncertainties related to regulatory application, review and approval processes and Alder's compliance with applicable legal and regulatory requirements; risks and uncertainties relating to the manufacture of eptinezumab; Alder's ability to obtain and protect intellectual property rights, and operate without infringing on the intellectual property rights of others; the uncertain timing and level of expenses associated with Alder's development and commercialization activities; the sufficiency of Alder's capital and other resources; market competition; changes in economic and business conditions; and other factors discussed under the caption «Risk Factors» in Alder's Annual Report on Form 10 - K for the fiscal year ended December 31, 2017, which was filed with the Securities and Exchange Commission (SEC) on February 26, 2018, and is available on the SEC's website at www.sec.gov.
Woo counters that Maastricht University in the Netherlands is currently
conducting a clinical
trial studying his company's supplements, which will publish at ClinicalTrials.gov.
In fact, one of Marathon's clinical
trials that the FDA used as part of its decision - making process was
conducted more than 20 years ago, saving the firm plenty of
study costs.
Over the next four years, Rodale Institute will
conduct a research project on Industrial Hemp through two field
trials, a Variety
Trial and Weed Suppression
Trial, and one greenhouse
study.
For the
study, Bonuck and her team
conducted two clinical
trials, one among low - income women and one among more economically diverse women.
Current research includes: co-leading organisational case
studies in Birthplace in England, a national
study of birth outcomes in home, midwife led, and obstetric led units; investigating the relationship between measures of safety climate and health care quality in A and E and intrapartum care; and
conducting nested process evaluations of two
trials of obesity in pregnancy behavioural interventions.
As it has been shown that
conducting a randomised controlled
trial is not possible, the best evidence about the safety of home birth can only come from good quality, routine registrations such as the one we used in our
study.
Hendrix et al: Moving on to section II, labeled Randomized Controlled
Trials (RCTs), I am once again wondering how RCTs can be ethically
conducted to
study birthplace.
Research shows that families typically receive roughly half of the number of home visits expected.16, 17 For example, across three randomized controlled
trials conducted of Nurse Family Partnership, average dosage of visits ranged from 45 to 62 percent.18 Research also shows that many, perhaps most, families enrolled in home visiting programs drop out before their eligibility ends.16, 19,20 Some home visiting
studies have varied the dosage that families were offered and found that fewer home visits produced outcomes similar to higher levels of exposure.21
Clinical
trials are
studies that are
conducted to see how one can «outgrow» a food allergy.
The objective of the current
study was to systematically review randomised controlled
trials of parenting programmes for the treatment of children with
conduct problems.
Eleven
studies were in
conducted in developing countries, including the two controlled
trials in Honduras, and 12 were in developed countries
To be included in this critical review,
studies had to be U.S. - based randomized
trials evaluating a breastfeeding promotion intervention, reporting breastfeeding outcome data, enrolling primarily minority participants, and
conducting analyses by intention to treat.
Such
trials should be
conducted in varied populations and settings and include longer periods of restricted exposure to pacifiers than have been examined thus far.13 Until such
studies can be completed, it is important that breastfeeding support and education be incorporated into prenatal obstetric and early pediatric patient encounters.
We
conducted our
study in conjunction with the clinical
trials and epidemiology research unit, which is an independent organisation funded by the National Medical Research Council.
Seven
studies [4
conducted in adults (6, 10, 11, 18) and 3
conducted in children (15, 30, 33); 5261 subjects in total; 6 observational
studies and 1
trial] reported on the association between infant feeding and fasting blood glucose in later life (Table 1 and Figure 3).
The 73
trials that contributed data to the analyses were
conducted in 29 countries; 52
studies (62.1 % of participants) in high - income countries, 15 (30.1 % of participants) in upper - middle income countries, four (3.4 % of participants) in lower - middle income countries, and four (4.4 % of participants) in low - income countries.
A formative
study using participatory action research design will first be
conducted, followed by a cluster - randomised
trial utilising both qualitative and quantitative data collection methods.
In the many responses to Gov. Cuomo's efforts to introduce formal and public teacher evaluation, teachers, union leaders and educational leaders have offered little but delaying tactics, such as more
study is needed or how about
conducting small
trials.
One of the best ways scientists have to prove cause and effect in medicine is to
conduct a randomized controlled
trial, in which
study subjects are randomly assigned to two groups.
In three randomized
trials, treatment of chronic low back pain with radiofrequency denervation, a procedure that can be performed with different techniques including the application of an electric current to the pain -
conducting nerve, resulted in either no improvement or no clinically important improvement in chronic low back pain, according to a
study published by JAMA.
In some 3000 elderly people, Nir Barzilai of the Albert Einstein School of Medicine in the Bronx, New York, and his colleagues plan to
conduct a
trial in which half the subjects would get a placebo and half would get an old (indeed, ancient) drug for type 2 diabetes called metformin, which has been shown to modify aging in some animal
studies.
This was caused by an erroneous and incomplete search by the manufacturer for
studies on the comparator therapy; no search at all was
conducted in
trial registries.
Additional tests — cognitive assessments, measurement of blood markers and MRI brain scans — were
conducted at the
trial's outset, at 6 months and at the end of the
study period.
Researchers who
conduct animal
studies often don't use simple safeguards against biases that have become standard in human clinical
trials — or at least they don't report doing so in their scientific papers, making it impossible for readers to ascertain the quality of the work, an analysis of more than 2500 journal articles shows.
The company plans in October to
conduct a separate test specifically to
study the seasonal flu vaccine's effectiveness among 480 elderly participants (a demographic often encouraged to get seasonal flu shots), and Phase III efficacy
trials across a larger set of demographics are scheduled to begin early next year.
Armed with the knowledge of how to
study vaccines appropriately, scientists ideally should have no trouble
conducting proper
trials.
To investigate this, the authors
conducted a
study involving participants of Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Re-lease Controlled Evaluation (ADVANCE)
trial (published in The Lancet in 2007 and the New England Journal of Medicine in 2008), with its cohort described by the authors as being generally representative of people with diabetes in developed countries such as Australia, New Zealand, China and nations of Europe, and also including China, a developing country.
And scientists who
conduct human challenge
studies, which typically involve a few dozen participants, say they have critical benefits: In addition to saving time and money, they can reveal harm caused by a potential drug or vaccine before it enters large - scale human efficacy
trials.
The
study conducted in Philadelphia is believed to be the first randomized controlled
trial to test inexpensive interventions that restore vacant urban land and reduce violence and fear among residents.
Northfield Laboratories, Inc., in Evanston, Ill., has been
conducting clinical
trials for its oxygen - carrying red blood cell substitute, PolyHeme, but in May said the product failed to meet the primary goals of mortality and safety in an important phase III
study.
«The current landscape of stem cell tourism should prompt a re-evaluation of current approaches to
study cell - based interventions with respect to the design, initiation and
conduct of U.S. clinical
trials,» the authors wrote.
Wyss - Coray, whose group did most of the mouse
studies that inspired the clinical
trial, now plans to
conduct a second, larger
trial using plasma from which many proteins and other molecules have been removed.
The new
study is a meta - analysis of three randomized controlled
trials conducted by the Alliance for Clinical Trials in Oncology (formerly Cancer and Leukemia Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GI
trials conducted by the Alliance for Clinical
Trials in Oncology (formerly Cancer and Leukemia Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GI
Trials in Oncology (formerly Cancer and Leukemia Group B)(CALGB) with support from the NCI, Intergroupe Francophone du Myélome (IFM), and the Gruppo Italiano Malattie Ematologiche dell «Adulto (GIMEMA).
It was originally designed to advance to a Phase 3
trial among 28,000 volunteers but was scaled back because the decline in new Ebola cases made it impossible to
conduct the larger
study.
Many of the
studies conducted are first - in - human
trials of experimental drugs or drug combinations that have shown promise in laboratory
studies.
The author
studied the effect of vitamin E on the risk of pneumonia in a large randomised
trial (Alpha - Tocopherol Beta - Carotene Cancer Prevention
Study — ATBC)
conducted in Finland between 1985 and 1993.
Independent of these preclinical
studies, Clementia Pharmaceuticals is currently
conducting phase 2 clinical
trials in individuals with FOP, based on the 2011 preclinical results published by Pacifici and Iwamoto.
Yet Bennett and her team had been anxious as their
study unfolded because AAV (like the early versions of engineered AdV) had previously failed to cure hemophilia in a
trial conducted by their Children's Hospital colleague, hematologist Kathy High.
He analyzed the data of the randomized
trial (Alpha - Tocopherol Beta - Carotene Cancer Prevention [ATBC]
Study) which was
conducted in Finland between 1985 - 1993 and included male smokers aged from 50 to 69 years.
The
study is the largest placebo - controlled
trial in older men
conducted on the subject to date.
A well
conducted randomized
trial is more likely to produce correct results, but a less rigorous
study might still satisfy a physician if the risks are low and its potential benefits are great, he says.
To get around that problem, this
study used the Bradford Hill criteria: a standard tool for assessing the impact of broad - based public health interventions where it is ethically not feasible or operationally impractical to
conduct randomized controlled
trials.
The evaluation of THN programs is challenging: randomized controlled
trials are often considered the gold standard of scientific
study, but
conducting trials for THN would often be unethical and fraught with difficulties given the infrequency and unpredictability of overdose.
Motivated by their previous finding of the presence of P - glycoprotein overexpression in the nasal lining of patients with CRS with nasal polyps, the
study authors
conducted a randomized, double - blind, placebo - controlled clinical
trial studying the use of low - dose Verapamil in 18 patients with CRS with nasal polyps.
The attendees developed a list of top research priorities and a research agenda for exercise in solid organ transplant, which includes the need to
conduct large multicenter intervention
studies, standardize measures of physical function in clinical
trials, examine the benefits of novel types of exercise, and assess the effects of exercise on measures such as immunity, infection, and cognition.
The
study was well done, she says, but teasing out effective treatments for social and medical problems is different from
conducting a drug
trial.
Yet clinical
trials in children commonly go either uncompleted or unpublished, finds a comprehensive
study conducted by researchers at Boston Children's Hospital.
Julia Lewis, MD (Vanderbilt University School of Medicine) and her colleagues in the Collaborative
Study Group
conducted a 441 - patient randomized clinical
trial to test the potential of a compound called ferric citrate to bind phosphorus, increase iron stores, and reduce the usage of IV iron and ESAs.