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Respiratory Diseases and Treatment

Clinical trials and the role of NICE

  • 3 things to know
  • Components 01, 02 and 03

Overview

Recall questions on phase I to IV clinical trials, sample size and representative samples, randomisation, placebos and double-blind trials, and the clinical practice, health technology and public health guidance of NICE, quality-adjusted life years and criticisms of its decisions.

What you need to know

Answer each one before you reveal it.

Your recallNot started
Key term

State the purpose of a phase I clinical trial and who takes part.

Key term

State the purpose of a phase II clinical trial.

Key term

Why must the people recruited to a trial be representative of the patients who will eventually take the drug?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    State the purpose of a phase I clinical trial and who takes part.

    Model answer

    A phase I trial tests safety, side effects and the dose range in a small group of usually healthy volunteers.

  2. 2

    State the purpose of a phase II clinical trial.

    Model answer

    A phase II trial tests whether the drug actually works in a few hundred patients who have the condition, and refines the best dose.

  3. 3

    Describe what happens in a phase III clinical trial.

    Model answer

    The drug is given to several hundred or several thousand patients at many centres and compared with a placebo or the current best treatment, using randomisation and blinding, to establish how effective it is and to detect less common side effects.

  4. 4

    Why is a phase IV trial carried out after a drug has been licensed?

    Model answer

    Because rare side effects and long-term effects only appear once very large numbers of ordinary patients have taken the drug for a long time.

  5. 5

    Explain why a large sample size is important in a clinical trial.

    Model answer

    A large sample reduces the effect of chance and of atypical individuals, allows any difference between the groups to be shown to be statistically significant, and makes it possible to detect rare side effects.

  6. 6

    Why must the people recruited to a trial be representative of the patients who will eventually take the drug?

    Model answer

    Age, sex and other conditions affect how a drug is handled by the body, so results from an unrepresentative sample cannot safely be applied to the wider population.

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