Research imperative
There is a note of caution expressed when clinical care providers enroll their own patients into investigational trials, a concern expressed in the called dual-role consent. There is concern that this circumstance may create a conflict of interest for the physician-investigator, lead to loss of pati...
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Format: | Article |
Language: | English |
Published: |
Elsevier
2019-06-01
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Series: | Contemporary Clinical Trials Communications |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2451865419300055 |
_version_ | 1818489169385619456 |
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author | Howard Trachtman |
author_facet | Howard Trachtman |
author_sort | Howard Trachtman |
collection | DOAJ |
description | There is a note of caution expressed when clinical care providers enroll their own patients into investigational trials, a concern expressed in the called dual-role consent. There is concern that this circumstance may create a conflict of interest for the physician-investigator, lead to loss of patient voluntarism, and promote the therapeutic misconceptions. In this opinion paper, I review the circumstances surrounding participation in clinical research and the conduct of standard patient care. I propose that when a patient is eligible for an institutional review board-approved clinical trial, instead of representing a potential ethical lapse, soliciting enrollment by the clinician-researcher may represent optimal care for the patient. |
first_indexed | 2024-12-10T17:00:13Z |
format | Article |
id | doaj.art-c428e730091043ad81d3f3f9b5071ba6 |
institution | Directory Open Access Journal |
issn | 2451-8654 |
language | English |
last_indexed | 2024-12-10T17:00:13Z |
publishDate | 2019-06-01 |
publisher | Elsevier |
record_format | Article |
series | Contemporary Clinical Trials Communications |
spelling | doaj.art-c428e730091043ad81d3f3f9b5071ba62022-12-22T01:40:34ZengElsevierContemporary Clinical Trials Communications2451-86542019-06-0114Research imperativeHoward Trachtman0403 E34th Street, Room 1-02, New York, NY, 10016, USA; Department of Pediatrics, Division of Nephrology, NYU, Langone Health, New York, NY, 10016, USAThere is a note of caution expressed when clinical care providers enroll their own patients into investigational trials, a concern expressed in the called dual-role consent. There is concern that this circumstance may create a conflict of interest for the physician-investigator, lead to loss of patient voluntarism, and promote the therapeutic misconceptions. In this opinion paper, I review the circumstances surrounding participation in clinical research and the conduct of standard patient care. I propose that when a patient is eligible for an institutional review board-approved clinical trial, instead of representing a potential ethical lapse, soliciting enrollment by the clinician-researcher may represent optimal care for the patient.http://www.sciencedirect.com/science/article/pii/S2451865419300055 |
spellingShingle | Howard Trachtman Research imperative Contemporary Clinical Trials Communications |
title | Research imperative |
title_full | Research imperative |
title_fullStr | Research imperative |
title_full_unstemmed | Research imperative |
title_short | Research imperative |
title_sort | research imperative |
url | http://www.sciencedirect.com/science/article/pii/S2451865419300055 |
work_keys_str_mv | AT howardtrachtman researchimperative |