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Overview and Purpose of this Guide to Clinical Trials in the NHS Overview and purpose of this guide | |
Who should use this guide to clinical trials in the NHS? | |
Clinical Trials Explained What are clinical trials? | |
Why are clinical trials needed? | |
Who is involved in a clinical trial? | |
How are clinical trials designed and approved? | |
Progression of a medical intervention through the clinical trial phases | |
Summary | |
Clinical Trial Approval, Regulation and Funding | |
How are clinical trials approved and regulated? | |
Ethical approval Informed consent | |
How are trials managed? | |
Who pays for a clinical trial? | |
Summary | |
Understanding Clinical Trial Design and Results | |
Understanding randomisation and blinding in clinical trials | |
Understanding controls and placebos | |
Why are placebos used in clinical trials? | |
What about trials that are not controlled or blinded? | |
Understanding clinical trial results | |
Summary | |
Questions About Clinical Trials: A Framework for Discussion | |
What are patients' rights? | |
Why do patients take part in clinical trials? | |
Why do patients decline to take part in a clinical trial or withdraw from a clinical trial they are involved in? | |
How can patients be empowered during their involvement in a clinical trial? | |
Will patients involved in clinical trials need extra help and support from their carers? | |
What are the likely costs of and reimbursement for patients participating in clinical trials? | |
Summary | |
Finding Out About Clinical Trials that are Currently or Soon to be Recruiting | |
ECRI Evidence Report: Patients' Reasons for Participation in Clinical Trials and Effect of Trial Participation on Patient Outcomes | |
Glossary | |
Index | |
Table of Contents provided by Publisher. All Rights Reserved. |
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