Literature DB >> 19901484

Informed Consent Documents submitted for initial review: what do they state about compensation for injured research participants?

S B Bavdekar1.   

Abstract

BACKGROUND: Research carries a small but definite risk of injury to participants. However, there is no unanimity amongst the stakeholders regarding the nature and extent of compensation to be provided to an injured participant. AIMS: To determine the extent to which issues related to the provision of free treatment and compensation for research-related injury are addressed in the protocols submitted to Ethics Committees (ECs). SETTING AND
DESIGN: Retrospective review of protocols submitted to two ECs in India.
MATERIAL AND METHODS: Initial protocols submitted to two ECs during the calendar years 2007 and 2008 were reviewed. Statements related to treatment and compensations for study-related injury were studied for adequacy regarding provisions for free emergency treatment, and free treatment and compensation for research-related injury. Presence of special conditions, exclusions, and caveats, if any, were noted. STATISTICAL ANALYSIS USED: The proportion of protocols providing free treatment and compensation for research-related injury was presented as a percentage.
RESULTS: The Informed Consent Documents (ICD) of 138 protocols were accessed. These included 115 (83.33%) industry-sponsored, 20 (14.49%) government-sponsored and three (2.17%) investigator-initiated projects. Forty-six (33.33%) intended to provide free treatment for a trial-related injury. Forty-two (30.43%) projects did not have any policy about providing treatment for a trial-related injury, whereas several others included statements that intended to provide treatment, but with certain restrictions. Thirty-three (23.91%) ICDs had statements indicating that there was no provision for compensation and 65(47.10%) ICDs stated nothing on the issue.
CONCLUSION: ICDs submitted for initial review are not in conformity with the provisions for treatment of and compensation for research-related injuries enunciated in national guidelines and draft guidelines.

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Year:  2009        PMID: 19901484

Source DB:  PubMed          Journal:  Indian J Med Sci        ISSN: 0019-5359


  3 in total

1.  What empirical research has been undertaken on the ethics of clinical research in India? A systematic scoping review and narrative synthesis.

Authors:  Sangeetha Paramasivan; Philippa Davies; Alison Richards; Julia Wade; Leila Rooshenas; Nicola Mills; Alba Realpe; Jeffrey Pradeep Raj; Supriya Subramani; Jonathan Ives; Richard Huxtable; Jane M Blazeby; Jenny L Donovan
Journal:  BMJ Glob Health       Date:  2021-05

2.  High rate of awarding compensation for claims of injuries related to clinical trials by pharmaceutical companies in Japan: a questionnaire survey.

Authors:  Chieko Kurihara; Hideo Kusuoka; Shunsuke Ono; Naoko Kakee; Kazuyuki Saito; Kenji Takehara; Kiyokazu Tsujide; Yuzo Nabeoka; Takuya Sakuhiro; Hiroshi Aoki; Noriko Morishita; Chieko Suzuki; Shigeo Kachi; Emiko Kondo; Yukiko Komori; Tetsu Isobe; Shigeru Kageyama; Hiroshi Watanabe
Journal:  PLoS One       Date:  2014-01-08       Impact factor: 3.240

Review 3.  Challenges in launching multinational oncology clinical trials in India.

Authors:  Kamal S Saini; Gaurav Agarwal; Ramesh Jagannathan; Otto Metzger-Filho; Monika L Saini; Khurshid Mistry; Raghib Ali; Sudeep Gupta
Journal:  South Asian J Cancer       Date:  2013-01
  3 in total

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