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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Evaluation of the Efficacy and Safety of LevoCept

ClinicalTrials.gov ID: NCT02882191

Public ClinicalTrials.gov record NCT02882191. 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 May 4, 2026, 2:51 PM EDT

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

Official title

Evaluation of the Effectiveness, Safety and Tolerability of LevoCept (Levonorgestrel-Releasing Intrauterine System) for Long-Acting Reversible Contraception

Study identification

NCT ID
NCT02882191
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sebela Women's Health Inc.
Industry
Enrollment
279 participants

Conditions and interventions

Conditions

Interventions

  • LevoCept Drug

Drug

Eligibility (public fields only)

Age range
18 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
Oct 31, 2016
Primary completion
Jul 16, 2018
Completion
Nov 11, 2020
Last update posted
Apr 22, 2026

2016 – 2020

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Essential Access Health-Berkeley Berkeley California 94710
Essential Access Health-Los Angeles Los Angeles California 90010
University of California Davis Health System Department of Obstetrics and Gynecology Sacramento California 95817
University Of Colorado Department of Obstetrics & Gyncology Aurora Colorado 80045
Healthcare Clinical Data, Inc. North Miami Florida 33161
Emory University School of Medicine Gynecology/Obstetrics Atlanta Georgia 30322
Kapiolani Medical Center for Women and Children Honolulu Hawaii 96826
Columbia University Medical Center New York New York 10032
University of Cincinnati Physicians Company, Inc Cincinnati Ohio 45267
Ohio State University Columbus Ohio 43209
Oregon Health & Science University Portland Oregon 97239
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104
Clinical Research of Philadelphia, LLC Philadelphia Pennsylvania 19114
Advanced Research Associates Corpus Christi Texas 78414
University of Utah Healthcare Health Sciences Center Salt Lake City Utah 84132
Seattle Women's: Health, Research, Gynecology Seattle Washington 98105

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 NCT02882191, 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 Apr 22, 2026 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02882191 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →