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Example 3.15 Protocol SQOLP01 (1999, Section 7): Comparison of steroid with cyclosporine for the topical treatment of oral lichen planus 7. Randomisation

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After the potential OLP case has been confirmed according to the eligibility criteria and informed consent has been obtained, the patient should be randomised.

To randomise a patient telephone
NMRC CLINICAL TRIALS & EPIDEMIOLOGY RESEARCH UNIT Tel: (65) 220‐1292, Fax: (65) 220‐1485 Monday–Friday: 0830 to 1730, Saturday: 0830 to 1230

Some brief details will be collected for identification purposes and the caller will be informed of the result of randomisation and at the same time the patient will be assigned a protocol Trial Number.

Randomised Clinical Trials

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