"Consent Forms" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Documents describing a medical treatment or research project, including proposed procedures, risks, and alternatives, that are to be signed by an individual, or the individual's proxy, to indicate his/her understanding of the document and a willingness to undergo the treatment or to participate in the research.
- Consent Forms
- Consent Form
- Informed Consent Documents
- Consent Document, Informed
- Consent Documents, Informed
- Document, Informed Consent
- Documents, Informed Consent
- Informed Consent Document
- Informed Consent Forms
- Informed Consent Form
- Consent Documents
- Consent Document
Below are MeSH descriptors whose meaning is more general than "Consent Forms".
Below are MeSH descriptors whose meaning is more specific than "Consent Forms".
This graph shows the total number of publications written about "Consent Forms" by people in this website by year, and whether "Consent Forms" was a major or minor topic of these publications.
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|Year||Major Topic||Minor Topic||Total|
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Below are the most recent publications written about "Consent Forms" by people in Profiles.
Legal Risks and Considerations Associated with Inflammatory Bowel Disease: A Primer. Am J Gastroenterol. 2018 11; 113(11):1577-1579.
A single consent for serial anesthetics in burn surgery. Anesth Analg. 2015 Jul; 121(1):219-222.
In Reply: Dr. Fine. Obstet Gynecol. 2014 Sep; 124(3):636.
Adding injury to injury: ethical implications of the Medicaid sterilization consent regulations. Obstet Gynecol. 2014 Jun; 123(6):1348-1351.
Informed consent for genetic research involving pleiotropic genes: an empirical study of ApoE research. IRB. 2006 Sep-Oct; 28(5):1-11.
Human subject protections in genetic research. Genet Test. 2004; 8(2):209-13.
Impact of therapeutic research on informed consent and the ethics of clinical trials: a medical oncology perspective. J Clin Oncol. 1999 May; 17(5):1601-17.
You can't always get what you want. Update. 1997 Jul; 13(2):5-7.
Pushing the envelope: informed consent in phase I trials. Ann Oncol. 1995 Apr; 6(4):321-3.
Statistical and ethical issues in the design and conduct of phase I and II clinical trials of new anticancer agents. J Natl Cancer Inst. 1993 Oct 20; 85(20):1637-43.