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Completed Phase 3 Interventional Results available

Clinical Safety Study of the Progesterone Vaginal Ring in Women Undergoing Assisted Reproductive Technology Procedures

ClinicalTrials.gov ID: NCT03565211

Public ClinicalTrials.gov record NCT03565211. 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 6, 2026, 2:12 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 Prospective, Multi-Center, Non-Comparative Trial of the Clinical Safety of the Progesterone Vaginal Ring in Women Undergoing Assisted Reproductive Technology (ART) Procedures

Brief summary

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

The purpose of the study is to assess the safety of Progesterone Vaginal Ring (PVR) in women undergoing fresh embryo transfer (ART).

Study identification

NCT ID
NCT03565211
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
352 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 34 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Jul 25, 2018
Primary completion
Jul 28, 2019
Completion
Jul 28, 2019
Last update posted
Nov 22, 2020

2018 – 2019

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Fertility Treatment Center Tempe Arizona 85284
HRC Fertility Encino California 91436
Reproductive Associates of DE Newark Delaware 19713
Women's Medical Research Group Clearwater Florida 33759
Center for Reproductive Medicine Winter Park Florida 32789
Idaho Center for Reproductive Medicine Boise Idaho 83702
InVia Fertility Hoffman Estates Illinois 60169
Carolina Conceptions Raleigh North Carolina 27607
Abington Reproductive Medicine Abington Pennsylvania 19046
Main Line Fertility Center Bryn Mawr Pennsylvania 19010
Center for Assisted Reproduction Bedford Texas 76022
Houston Fertility Institute Houston Texas 77063
Center of Reproductive Medicine Webster Texas 77598
Utah Fertility Center Pleasant Grove Utah 84062
Eastern Virginia Medical School | EVMS Obstetrics & Gynecology 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03565211, 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 Nov 22, 2020 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03565211 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →