Sentences with phrase «clinical trial sites include»

Collateral benefits to clinical trial sites include equipment and facilities, skills development, high - quality jobs for local researchers, healthcare workers and other staff, and generally a higher standard of healthcare for trial participants.

Not exact matches

The researchers conducted a randomized, multicenter, clinical trial that included 1,000 Chinese women with PCOS at 21 sites in China.

In one analysis that included 21 randomized clinical trials, investigators found a risk of 138 surgical site infections per 1000 procedures, and the use of sutures coated with the antimicrobial triclosan reduced this by 39.

The study included 124 newly diagnosed patients at 25 clinical trial sites in the U.S. Two - thirds of the patients were treated with ICT - 107, an experimental vaccine based on immune system cells called dendritic cells that were exposed to six synthetic proteins, or antigens, known to be involved in GBM development.

«Secondary benefits of this trial include the significant improvement in clinical care for children with sickle cell disease at each of the 29 sites because each location had a designated hematologist, neurologist, neuroradiologist and psychologist working as a team to identify and decrease further injury to the brain in this vulnerable population.»

Several human clinical trials began last fall at test sites including BIDMC, WRAIR, and National Institute of Allergy and Infectious Diseases affiliated clinical trial sites.

The white paper recommends that practitioners follow relevant guidance documents and that deviation from consensus recommendations should be supported by clinical studies or pursued in the setting of a clinical trial approved by an institutional review board; that practitioners receive training in a new procedure before beginning its practice, that the training should include a practical, «hands - on» component and that all team members directly involved with the radiation therapy decisions should participate in at least five proctored cases before performing similar procedures independently; and that professional societies should accelerate the generation of new or updated guidance documents for the following disease sites and techniques: skin, central nervous system, gastrointestinal, lung or endobronchial and esophagus, and, while outside the charge of this panel, assess the need for updated guidance documents for accelerated partial breast irradiation using electronic brachytherapy.

Many factors may cause differences between current expectations and actual results including unexpected safety or efficacy data observed during preclinical or clinical studies, clinical trial site activation or enrollment rates that are lower than expected, changes in expected or existing competition, changes in the regulatory environment, failure of Syndax's collaborators to support or advance collaborations or product candidates and unexpected litigation or other disputes.

The authors of the current study conducted a randomized, multicenter, clinical trial that included 1,000 Chinese women with PCOS at 21 sites in China.

Q: In 1995 you co-founded the Northeast ALS Consortium, a clinical trials network that has grown to include more than 100 academic sites worldwide.

The new network is also taking steps to standardize the prioritization of new studies and to put in place a unified system — including a central institutional review board that will cover studies conducted by the entire system — to protect research subjects at more than 3,000 clinical trial sites.

In 2005, Dan co-founded and served as President and CEO of Inviragen Inc., which he transformed from a virtual start - up to a global clinical stage company with sites in Colorado, Wisconsin and Singapore and translated two vaccines from the research bench to human clinical trials, including one for dengue fever.

Various on - line dating sites claim that their methods for pairing individuals produce more frequent, higher quality, or longer lasting marriages, but the evidence underlying the claims to date has not met conventional standards of scientific evidence including: (i) sufficient methodological details to permit independent replication; (ii) open and shared data to permit a verification of analyses; (iii) the presentation of evidence through peer - reviewed journals rather than through Internet postings and blogs; (iv) data collection free of artifacts, such as expectancy effects, placebo effects, and confirmatory biases by investigators; and (v) randomized clinical trials (3, 9).

Assisted seven clinical study teams in the execution of clinical trials, including the following activities: developed and maintained tracking tools, prepared minutes from meetings, prepared mailings to investigational sites, assisted with investigational site payments and budget oversight, inputted drug orders, randomized patients, and performed other study specific projects per the needs of the study team

Key Accomplishments • Created and implemented a clinical investigation plan which increased efficiency by 50 % • Trained 15 research assistants in handling site initiation, closeout and interim monitoring work • Introduced 8 different clinical trial committees, including clinical events committee, data safety monitoring board and steering committee • Obtained 3 informed consents for human research subjects which were in limbo for 5 years

The rationale, methods, and design of the trial have been detailed elsewhere.11 - 13 Clinical sites included primary care and outpatient psychiatric care settings serving public - or private - sector patients.

Clearly, more research is needed to understand how practices adapt operational and financial strategies for sustaining key program resources, including focused training and technical assistance through the Replicating Effective Programs (REP) program, 42 as well as discussions with state and local providers and stakeholders on a reimbursement model for care management activities so the clinics can absorb the costs.43 It is important to point out that the participating pediatric practices in this clinical trial later hired their own clinicians for on - site services after the trial had ended.