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Clinical research trials require written informed consent to safeguard the child’s best interest. Integrity of the process of consent is a matter of great concern.1 Formal training of the person taking consent in legal and ethical way, basic level of education of parents and information given about the trial, all play important role. Whether the parents are able to process the information correctly, under the stressful condition and are able to take decision of informed consent, needs to be evaluated.2 Moreover, it is important to understand that making decision about the child, needs parents enrollment and it can’t be left solely to doctor.3

Neonatal research: Parent’s perception of informed consent