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The questionnaire can be completed by any woman undergoing investigation for symptoms of endometriosis (whether she has the disease or not), or asymptomatic women, subject to signed written informed consent obtained from each patient and local ethics approval for the study according to ethical principles for clinical research summarized in the Declaration of Helsinki.
All questionnaires and SOPs produced by the WERF EPHect Working Group are freely available for use by investigators, subject to signed written informed consent obtained from each patient and local ethical approval for the study according to ethical principles for clinical research as summarized in the Declaration of Helsinki.
All questionnaires and SOPs produced by the WERF EPHect Working Group are freely available for use by investigators, subject to signed, written, informed consent obtained from each patient, and local ethical approval for the study according to ethical principles for clinical research summarized in the Declaration of Helsinki.
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Verbal consent was obtained because of the high rate of illiteracy and inability of subjects to sign their name.
The in-charge nurse was responsible for reminding the part time subjects to sign the badges in and out to prevent potential loss.
The DEG for each brain region was subjected to signed-WGCNA.
In addition, the subject has to sign the informed consent for participation in the study at this point.
Each recruited subject has to sign an informed consent form.
Each recruited subject has to sign a consent form and give their consent to randomisation.
In addition, each subject had to sign or thumbprint a patient consent form before they could be admitted into the study.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com