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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Compare Two Copper IUDs: Mona Lisa NT Cu380 Mini and ParaGard

ClinicalTrials.gov ID: NCT03124160

Public ClinicalTrials.gov record NCT03124160. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 10:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center, Single-blind, Randomized Clinical Trial to Compare Two Copper IUDs: Mona Lisa NT Cu380 Mini and ParaGard

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This will be a multi-site, participant-blinded, randomized clinical trial. The investigators will randomize 1000 eligible participants in a 4:1 ratio to two different copper IUDs: 800 to Mona Lisa NT Cu380 Mini and 200 to ParaGard.

Study identification

NCT ID
NCT03124160
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
FHI 360
Other
Enrollment
1,105 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years to 40 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 25, 2017
Primary completion
Jun 5, 2022
Completion
Jun 5, 2022
Last update posted
Sep 24, 2024

2017 – 2022

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Essential Access Health Los Angeles California 90010
University of California, Davis Sacramento California 95817
University of California, San Francisco San Francisco California 94110
University of Colorado Denver Colorado 80045
University of Hawaii Honolulu Hawaii 96826
Johns Hopkins University Baltimore Maryland 21224
Boston Medical Center Corporation Boston Massachusetts 02118
Planned Parenthood League of Massachusetts Boston Massachusetts 02215
Planned Parenthood of New York New York New York 10012
Columbia University New York New York 10032
University of Cincinnati Cincinnati Ohio 45267
Oregon Health & Science University Portland Oregon 97239
University of Pennsylvania Philadelphia Pennsylvania 19104
University of Pittsburgh Pittsburgh Pennsylvania 15213
University of Utah Salt Lake City Utah 84106
Eastern Virginia Medical School Norfolk Virginia 23507

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03124160, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 24, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03124160 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →