Since 2006, the number of industry -
sponsored clinical trials studying the benefits and harms of medical treatments has risen dramatically, while the number of clinical trials funded by the National Institutes of Health (NIH) has fallen substantially, according to new Johns Hopkins Bloomberg School of Public Health research.
HIGHLIGHTS OF QUALIFICATIONS * Over 4 + years of progressive work experience in clinical and academic research hospital settings, collaborating with investigators and a multidisciplinary health care team in the recruitment of study participants for various investigator - initiated and industry
sponsored clinical trial studies.
Not exact matches
The researchers were never able to obtain the data from the original
clinical trial sponsor and in the end had to painstakingly reconstruct the
study results from the information collected at each individual
study site.
The 21 - patient
study,
sponsored by the nonprofit Multidisciplinary Association for Psychedelic
Studies (MAPS), launched in 2004 as the first U.S.
clinical trial of a psychedelic drug in 35 years.
Data from the CenterWatch
study indicate that over 70 % of
clinical trial sponsors and service providers feel that the adoption of electronic data collection would be more rapid absent the fear of regulatory repercussions.
The drug is not approved for weight management, according to its manufacturer, Denmark - based Novo Nordisk, which
sponsored this
study, called the SCALE ™ (Satiety and
Clinical Adiposity - Liraglutide Evidence in Nondiabetic and Diabetic Subjects) Obesity and Prediabetes
trial.
Aggressive treatment of high blood pressure comes with risks, and the
study, a large
clinical trial sponsored by the National Institutes of Health, has not yet been peer - reviewed or published.
It's essential that people feel they are in a safe, comfortable setting with someone who can oversee the experience, says Alicia Danforth, a
clinical psychologist at the Harbor — UCLA Medical Center in Torrance, California, who is involved in MAPS -
sponsored trials studying MDMA's effects on social anxiety in adults with autism.
We
sponsor clinical trials for newly diagnosed neuroblastoma patients through the Children's Oncology Group (COG) and, through COG and the New Approaches to Neuroblastoma Therapy Consortium, Dana - Farber / Boston Children's offers the most Phase I
clinical studies in New England for children whose disease has recurred.
Studies may involve laboratory or clinical investigation, including genetic studies, but the Program will not sponsor therapeutic
Studies may involve laboratory or
clinical investigation, including genetic
studies, but the Program will not sponsor therapeutic
studies, but the Program will not
sponsor therapeutic
trials.
www.DupCheck.org is a web - based tool to screen for duplicate patients in
clinical trials within and across
studies,
sponsors and therapeutic areas.
The National Cancer Institute and the National Center for Complementary and Integrative Health (NCCIH) are
sponsoring a number of
clinical trials (research
studies) at medical centers to test CAM therapies for use in cancer.
To accomplish our mission, we serve as a «one - stop - shop» for our veterinary faculty, other campus units and
study sponsors by providing
clinical technical expertise, administrative support and financial oversight for small and large animal
clinical trials in multiple disciplines, including (but not limited to) ophthalmology, oncology, neurology, cardiology, dermatology, diagnostic imaging, dentistry, internal medicine, orthopedics and soft tissue surgery.
A
Clinical Trial Agreement specifies what product (for example, the
study drug or device) the
sponsor will provide the institution, as well as any financial support, and / or proprietary information.
-- Updated case reports and source documents for
clinical trials, arranged
study interviews, and recruitment — Updated medical records, maintained information on protocol and case reports for each
trial, developed flow sheets and identified subject eligibility — Performed QA / QC procedures, worksheets and
study materials, collected data and ordered supplies — Prepared consent amendments and processed specimens — Prepared
sponsor files for FDA compliance and GCP guidelines
Differences in reporting serious adverse events in industry
sponsored clinical trial registries and journal articles on antidepressant and antipsychotic drugs: a cross-sectional
study