 Informed Consent
"Informed Consent" 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.
Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.
| Descriptor ID |
D007258
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| MeSH Number(s) |
I01.880.604.473.650.718 I01.880.604.583.427 N03.706.437.650.312 N03.706.535.489
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Informed Consent".
Below are MeSH descriptors whose meaning is more specific than "Informed Consent".
This graph shows the total number of publications written about "Informed Consent" by people in this website by year, and whether "Informed Consent" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 0 | 1 | 1 | | 2016 | 0 | 1 | 1 | | 2017 | 1 | 1 | 2 | | 2019 | 0 | 1 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Informed Consent" by people in Profiles.
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Chapman CR, Quinn GP, Natri HM, Berrios C, Dwyer P, Owens K, Heraty S, Caplan AL. Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision? Am J Bioeth. 2025 Feb; 25(2):47-60.
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Faseru B, Mussulman LM, Nazir N, Ellerbeck EF, Shergina E, Scheuermann TS, Gajewski BJ, Catley D, Richter KP. Use of pre-enrollment randomization and delayed consent to maximize participation in a clinical trial of opt-in versus opt-out tobacco treatment. Subst Abus. 2022; 43(1):1035-1042.
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Abdel-Rahman SM. Facilitating Informed Permission/Assent/Consent in Pediatric Clinical Trials. Paediatr Drugs. 2019 Aug; 21(4):205-214.
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Shakhnovich V, Hornik CP, Kearns GL, Weigel J, Abdel-Rahman SM. How to Conduct Clinical Trials in Children: A Tutorial. Clin Transl Sci. 2019 05; 12(3):218-230.
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Wong CS, Kogon AJ, Warady BA, Furth SL, Lantos JD, Wilfond BS. Ethical and Policy Considerations for Genomic Testing in Pediatric Research: The Path Toward Disclosing Individual Research Results. Am J Kidney Dis. 2019 06; 73(6):837-845.
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Sabatello M, Janvier A, Verhagen E, Morrison W, Lantos J. Pediatric Participation in Medical Decision Making: Optimized or Personalized? Am J Bioeth. 2018 03; 18(3):1-3.
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Berrios C, James CA, Raraigh K, Bollinger J, Murray B, Tichnell C, Applegate CD, Bergner AL. Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results. J Genet Couns. 2018 02; 27(1):263-273.
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Fowler SA, Saunders CJ, Hoffman MA. Variation among Consent Forms for Clinical Whole Exome Sequencing. J Genet Couns. 2018 02; 27(1):104-114.
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Khoo EJ, Schremmer RD, Diekema DS, Lantos JD. Ethical Concerns When Minors Act as Standardized Patients. Pediatrics. 2017 Mar; 139(3).
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Feltman DM, Lantos JD. Neonatologists' opinions about the 'foreseeable risks' in comparative effectiveness research: Results from an online survey. J Perinatol. 2017 03; 37(3):311-314.
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