Ghislaine van Thiel

Associate professor Medical Ethics

University Medical Center Groningen

Netherlands

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About

Ghislaine van Thiel is an Associate Professor of Medical Ethics at the University Medical Center Utrecht, Netherlands. Her research focuses on the ethical considerations in decentralized clinical trials, informed consent, and the implications of data-intensive health research governance. She has published extensively on topics such as the risks and benefits of research, euthanasia, and the application of brain-computer interfaces in healthcare.

Articles (13)

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2025

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2024

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2024

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (8)

Sam Muller

Assistant professor

University Medical Center Groningen

NETHERLANDS

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Dipak Kotecha

University of Birmingham

UNITED KINGDOM

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Isla Mackenzie

Academic, Clinical Professor (Teaching and Research) of Cardiovascular Medicine

University of Dundee

UNITED KINGDOM

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Carlo Leget

Professor

University of Humanistic Studies

NETHERLANDS

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Amos de Jong

Utrecht University

NETHERLANDS

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Helga Gardarsdottir

Associate professor

Utrecht University

NETHERLANDS

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Barbara Casadei

University of Oxford

UNITED KINGDOM

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Mira Zuidgeest

University Medical Center Utrecht, Utrecht University

NETHERLANDS

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Ghislaine van Thiel

Research Interests

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About

Articles (13)

Which Benefits Can Justify Risks in Research? Response to Open Peer Commentaries

Which Benefits Can Justify Risks in Research?

The Ethics of Decentralized Clinical Trials and Informed Consent: Taking Technologies’ Soft Impacts into Account

Towards clinical application of implantable brain–computer interfaces for people with late-stage ALS: medical and ethical considerations

Requests for euthanasia or assisted suicide of people without (severe) illness

Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

A cross-sectional survey on the early impact of COVID-19 on the uptake of decentralised trial methods in the conduct of clinical trials

CODE-EHR best practice framework for the use of structured electronic healthcare records in clinical research

CODE-EHR best practice framework for the use of structured electronic healthcare records in clinical research

Ethics review of decentralized clinical trials (DCTs): Results of a mock ethics review

Learning accountable governance: Challenges and perspectives for data-intensive health research networks

Lifelong versus not lifelong death wishes in older adults without severe illness: a cross-sectional survey

A Response to a Letter of Vivat and Twycrossrs information

Collaborators (8)

Sam Muller

Dipak Kotecha

Isla Mackenzie

Carlo Leget

Amos de Jong

Helga Gardarsdottir

Barbara Casadei

Mira Zuidgeest

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