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The Experts below are selected from a list of 13044 Experts worldwide ranked by ideXlab platform

Christopher D. Hillyer - One of the best experts on this subject based on the ideXlab platform.

Xavier Carné - One of the best experts on this subject based on the ideXlab platform.

  • Who is willing to participate in low-risk pragmatic clinical trials without consent?
    European journal of clinical pharmacology, 2017
    Co-Authors: Rafael Dal-ré, Antonio J. Carcas, Xavier Carné
    Abstract:

    Purpose General notification offers a possible alternative to written informed consent for pragmatic randomized controlled trials (pRCTs). It involves patients being informed through brochures, posters, and letters that research is being conducted simultaneously to providing clinical care and that patients will be enrolled in pRCTs without study-specific consent. A previous survey found that a Substantial Minority of respondents endorsed general notification. We aimed to know who is willing to enroll in this type of trials using general notification rather than written consent.

Megan Griffith - One of the best experts on this subject based on the ideXlab platform.

Ezekiel J Emanuel - One of the best experts on this subject based on the ideXlab platform.

  • patients views on financial conflicts of interest in cancer research trials
    The New England Journal of Medicine, 2006
    Co-Authors: Lindsay A Hampson, Manish Agrawal, Steven Joffe, Cary P Gross, Joel Verter, Ezekiel J Emanuel
    Abstract:

    BACKGROUND Financial ties between researchers or medical centers and companies whose drugs are being tested have come under increasing scrutiny. METHODS We conducted in-person interviews with 253 patients in cancer-research trials (a 93% response rate) at five U.S. medical centers to determine their attitudes regarding potential financial conflicts of interest among researchers and medical centers. RESULTS More than 90% of patients expressed little or no worry about financial ties that researchers or institutions might have with drug companies. Most patients said they would have enrolled in the trial even if the drug company had paid the researcher for speaking (82% of those interviewed) or consulting (75%) or if the researcher had received royalty payments (70%) or owned stock in the company (76%). Similarly, most patients would have enrolled in the trial if their cancer center had owned stock in the drug company (77%) or received royalty payments from the company (79%). Most patients believed it was ethical for researchers to receive speaking fees (81%) or consulting fees (82%) from the company. However, a Substantial Minority of patients wanted disclosure of the oversight system for researchers (40%) and of researchers' financial interests (31%); 17% thought no disclosure to patients was necessary. CONCLUSIONS Most patients in cancer-research trials were not worried about financial ties between researchers or medical centers and drug companies and would still have enrolled in the trial if they had known about such financial ties. A Substantial Minority wanted to be informed about the oversight system to protect against financial conflicts of interest and about researchers' financial interests.

Enrica Morra - One of the best experts on this subject based on the ideXlab platform.