Clinical Trial

A Reduced Dose of Cabergoline for Lactation Inhibition After Second-Trimester Abortion or Pregnancy Loss

Study acronym: LISTA3
Withdrawn Phase 2
View on ClinicalTrials.gov →
Why the trial stopped
Lack of funding
Summary
Most patients seeking abortion care or management of pregnancy loss in the second trimester will lactate, which can be physically and emotionally painful. The efficacy of a one-time dose of cabergoline has been previously demonstrated to prevent breast symptoms for these patients. This study seeks to determine if investigators can more precisely manage these patients with a reduced dose appropriate for the physiology of the second trimester, thereby reducing the medication cost and reducing or eliminating the uncomfortable medication side effects.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-03-27; most recent amendment 2026-07-15.
Status change: Not Yet Recruiting → Withdrawn 2026-07-15
Trial Details
NCT Number NCT06909123
Lead Sponsor Stanford University
Conditions Lactation Suppressed
Start Date 2026-07
Primary Completion 2027-01 (estimated)
Study Completion 2027-07 (estimated)
Updated on ClinicalTrials.gov 2026-07-17