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Study identifier: NCT06123026 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pharmacological Inhibition of Lactation After 16 to 20 Week Abortion

Condition: Lactation Suppressed · Second Trimester Abortion  ·  Sponsor: Northwestern University

PhasePhase 4
Planned participants200
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to compare breast symptoms (lactation, engorgement, etc) of individuals who undergo a procedure for second trimester of pregnancy loss between 16 weeks and 20 weeks gestational age. The participants will be randomly placed in two groups, one with a placebo tablet and one with medication called "cabergoline" which are taken immediately after their procedure. Researchers will compare groups to see if there are any significant differences in breast symptoms.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (1)

Northwestern Medical CenterChicago, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06123026