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Therapeutic optimism in the consent forms of phase 1 gene transfer trials: an empirical analysis

Therapeutic optimism in the consent forms of phase 1 gene transfer trials: an empirical analysis

http://www.wikidata.org/entity/Q35429376

about

The myth of equipoise in phase 1 clinical trials Accepting risk in clinical research: is the gene therapy field becoming too risk-averse?Using digital multimedia to improve parents' and children's understanding of clinical trials Therapeutic Misconception in Psychiatry Research: A Systematic Review.Can patient decision aids help people make good decisions about participating in clinical trials? A study protocol The therapeutic misconception: not just for patients.Patients' perception of the informed consent process for neurooncology clinical trials The role of therapeutic optimism in recruitment to a clinical trial in a peripartum setting: balancing hope and uncertainty.Research ethics application: a guide for the novice researcher.Zinc finger nucleases: looking toward translation.Ethical guideposts to clinical trials in oncology.Fully informed consent is impossible in surgical clinical trials.Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophy.Emotional impact of a paediatric exon-skipping therapy trial.

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P2860

Therapeutic optimism in the consent forms of phase 1 gene transfer trials: an empirical analysis

http://www.wikidata.org/entity/Q35429376

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2005 nî lūn-bûn

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2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2005 թվականի ապրիլին հրատարակված գիտական հոդված

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Kimmelman J

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Palmour N

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P2860

Quality of informed consent in cancer clinical trials: a cross-sectional survey.

False hopes and best data: consent to research and the therapeutic misconception.

Defining and describing benefit appropriately in clinical trials.

Ethical issues in phase I oncology research: a comparison of investigators and institutional review board chairpersons.

Responses and toxic deaths in phase I clinical trials.

Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial.

Genetic research as therapy: implications of "gene therapy" for informed consent.

Perceptions of cancer patients and their physicians involved in phase I trials.

What patients say about medical research.

Uncertain benefit: investigators' views and communications in early phase gene transfer trials.

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