CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 69 enrolled
Drug / intervention
Cabergoline 1 MG +1 moredrug
Likely dose
Cabergoline 1 MGfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06029673
NCT06029673Phase 2Completed

Cabergoline for Lactation Inhibition After Early Second-Trimester Abortion or Pregnancy Loss: A Randomized Controlled Trial

Stanford University·interventional·Posted Sep 8, 2023·Updated Oct 3, 2025

In Brief

A Phase 2 clinical trial evaluating Cabergoline 1 MG and Placebo for Lactation Suppressed. Completed, enrolled 69 participants across 2 sites.

Detailed Summary

Breast pain following second-trimester abortion is common. Breast engorgement and milk leakage following second-trimester perinatal loss and abortion can cause both physical pain and emotional distress. Dopamine agonists have previously been shown to be effective in lactation inhibition for third-trimester fetal/neonatal loss or contraindications to breastfeeding. The investigator's prior work demonstrated that compared to placebo, a single dose of cabergoline was effective in preventing breast symptoms after abortion or loss 18-28 weeks. As lactogenesis starts as early as 16 weeks gestation, the investigators hope to determine the efficacy of cabergoline earlier in the second trimester,16-20 weeks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
202420252026
First PostedSep 8, 2023
Enrollment StartFeb 7, 2024
Primary CompletionJun 15, 2025
Study CompletionJul 1, 2025
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 2.8 years ago

Interventions

Cabergoline 1 MGdrug

Dopamine agonist

Placebodrug

Placebo