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Clinical Trial Summary

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).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04038749
Study type Interventional
Source Zelazna Medical Centre, LLC
Contact Alicja Misztal, MSc
Phone +48 513 007 355
Email alicja.misztal@gmail.com
Status Recruiting
Phase N/A
Start date June 16, 2019
Completion date December 31, 2022

See also
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Enrolling by invitation NCT06029673 - Cabergoline for Lactation Inhibition After Early Second-Trimester Abortion or Pregnancy Loss Phase 2
Completed NCT05024422 - Lactation Inhibition, the Efficiency of Vitamin B6 Versus Cabergoline N/A
Recruiting NCT06123026 - Pharmacological Inhibition of Lactation After 16 to 20 Week Abortion Phase 4
Completed NCT04701333 - Cabergoline for Lactation Inhibition After Second-Trimester Abortion or Loss Phase 2