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Written informed consent is requested from all patients prior to participation in the study.
In research, it is common practice that extensive informed consent is requested, whereas traditionally, there is no (or little) feedback of results.
A written informed consent is requested concerning participation in the study, employment data from the employers' records, as well as dates and diagnoses of SA from the medical records of the OHS.
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A trial nurse responsible for obtaining informed consent was requested to present standard informed consent information on the microbicide study to the 18 women in the non-intervention group, in addition to health information on cervical cancer, and was advised to allow the women to ask questions.
Informed consent was requested at the start of the questionnaire.
The informed consent was requested from each of personnel who were involved in the study.
Following interviews, further informed consent was requested to access medical records.
For minors, the informed consent was requested from their parents/guardians.
As the patient recovered consciousness, deferred informed consent was requested from the patient.
Depending on the national requirements, written or oral informed consent was requested.
Informed consent was requested from the study subjects, or from the parents of patients.
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