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RECRUITING
NCT06123026
PHASE4

Pharmacological Inhibition of Lactation After 16 to 20 Week Abortion

Sponsor: Northwestern University

View on ClinicalTrials.gov

Summary

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.

Official title: Pharmacological Inhibition of Lactation After 16 to 20 Week Abortion: a Randomized Controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2023-12-18

Completion Date

2024-06-30

Last Updated

2024-05-29

Healthy Volunteers

Yes

Interventions

DRUG

Cabergoline

1mg oral cabergoline given to participants once

DRUG

Placebo

1 encapsulated placebo tablet given to participants after procedure

Locations (1)

Northwestern Medical Center

Chicago, Illinois, United States