TableĀ 6

Responses to statements about informed consent in clinical trials

Response: number (per cent)
Strongly agreeAgreeNeutralDisagreeStrongly disagree
It is important the patients give informed, written consent before being enrolled into any clinical trial24 (25%)48 (50%)14 (15%)10 (10%)0 (0%)
It is acceptable in some circumstances (eg, unconscious patients, resuscitation techniques) for patients to be randomised before consent10 (10%)49 (51%)17 (18%)14 (15%)6 (6%)
Obtaining consent from a relative is an ethically acceptable method of gaining consent2 (2%)35 (37%)23 (24%)31 (32%)5 (5%)
If paramedics or ambulance stations (rather than patients) are randomised, consent is not needed as there is no treatment choice at that time7 (7%)21 (22%)22 (23%)40 (42%)6 (6%)
If an ethics committee had approved the trial protocol for recruiting patients, I would be happy to follow it15 (16%)61 (64%)14 (15%)4 (4%)1 (1%)