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Evaluate the prevalence of exclusive breastfeeding at M3 within the Martigues CH.
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After delivery, the investigating midwife or investigating pediatrician can go to the room where the new mother is installed to present the study to her. Once the patient consents, an information note will be given to her after signing a non-opposition.
The investigator or designated caregiver will produce the hetero-questionnaire in paper form to be completed depending on the patient's availability.
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Central trial contact
sandrine MORITZ, Sage femme; Gwladys M'BOUNGOU Clinical Research cordonator, Master's degree
Data sourced from clinicaltrials.gov
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