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When a patient has been randomised you will be presented with one of the two screens below displaying which arm the patient has been randomised to:

Flexicult Arm

 Standard Care

Once a patient has been randomised please complete the randomisation  details on CRF 03, to indicate the patient’s study allocation.

Please ensure this page is signed and dated by the person conducting the randomisation

If you have any problems with the randomisation programme, please contact a member of the study  team whose details can be found in the study manual or the Contact Us page.