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Where problems or incidents were reported that were identified by the research staff as safety critical and requiring an immediate response, the patient was informed that the information would be passed on to the person in charge.
Every patient was informed about study protocol and procedures and signed informed consent form.
Each patient was informed of the nature of the study and signed an informed consent form.
Every patient was informed of the subject of the study, and a written informed consent obtained, following the tenets of the Declaration of Helsinki.
Each patient was informed on the nature of the study and signed the informed consent form.
Each patient was informed in advance about the study protocol in written form (informed consent) and verbal.
The patient was informed that data concerning the case would be submitted, and he consented.
When the latter was ≥4000 g the patient was informed about the risks of birth trauma.
Our patient was informed that data concerning his case would be submitted for publication.
This patient was informed of the side effects of long-term indwelling catheter drainage.
The patient was informed about his pathology and advised to undergo surgery.
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CEO of Professional Science Editing for Scientists @ prosciediting.com