The aim of the study is to improve the standard of care in case of the inhibition of lactation. The participant qualified for the study will answer the questions contained in the survey. The patient will have her breast palpated and then will be instructed on the possible options for the inhibition of lactation. The participant, who decides to inhibit lactation with medications, will be consulted by a doctor. Each patient will receive information of the possible ways to relieve the symptoms of overfilled breast and be able to contact with lactation consultant. The participant will also receive a card to assess the severity of symptoms in the following days. The investigators will call the patient between the third and fifth day by phone. Once again, after 2 weeks from the beginning of the inhibition of lactation in order to ask questions contained in the survey (the course of the process, problems that occurred and the level of satisfaction with the chosen method).
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Visual Analogue Scale (VAS)
Timeframe: from the 1st day of the inhibition of lactation to 14th day of process
Evaluation of breast status
Timeframe: from the 1st day of the inhibition of lactation to 14th day of process
Symptoms in association with the ingestion of medicines that inhibit lactation.
Timeframe: from the 1st day of the inhibition of lactation to 14th day of process
Breast palpation
Timeframe: 1st day of including in the study
Survey: 1st day of including in the study
Timeframe: 1st day of including in the study