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COMPLETED

Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine

NCT02513043 · View on ClinicalTrials.gov ↗

Study Summary

This pilot study is designed to obtain preliminary data on the safety, acceptability, and feasibility of direct-to-consumer telemedicine abortion.

Conditions Studied

Interventions

  • DRUG medical abortion

Study Locations (17)

New York

  • Choices Women's Medical Center — Jamaica
  • Maine Family Planning — New York

Oregon

  • Planned Parenthood Columbia Willamette — Portland
  • Oregon Health and Sciences University Women's Health Research Unit — Portland

Washington

  • Planned Parenthood Columbia Willamette — Washington
  • Oregon Health and Sciences University Women's Health Research Unit — Washington

Colorado

  • Planned Parenthood of the Rocky Mountains — Denver

District of Columbia

  • Carafem — Washington D.C.

Georgia

  • Carafem — Atlanta

Hawaii

  • The University of Hawaii Women's Options Centers — Honolulu

Illinois

  • Carafem — Skokie

Trial Details

FieldValue
Enrollment Target 1,470 participants
Start Date 2016-03-22
Est. Completion 2021-05-11

Sponsor

Gynuity Health Projects

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02513043

The ClinicalTrials.gov registry entry for NCT02513043 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,470 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gynuity Health Projects, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Pregnancy appearing as the primary indexed condition, and to 1 intervention — of which medical abortion is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02513043 reports 17 study locations spanning 14 distinct geographic areas — top geographies include New York, Oregon, Washington. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02513043 about?

NCT02513043 is a clinical study titled "Feasibility of Medical Abortion by Direct-to-Consumer Telemedicine". This pilot study is designed to obtain preliminary data on the safety, acceptability, and feasibility of direct-to-consumer telemedicine abortion.

What is the current status of trial NCT02513043?

This trial is currently completed. The enrollment target is 1,470 participants. The study started on 2016-03-22. Estimated completion is 2021-05-11.

What conditions does trial NCT02513043 study?

This clinical trial studies the following conditions: Pregnancy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02513043?

The interventions under investigation include: medical abortion (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02513043?

This trial is sponsored by Gynuity Health Projects, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02513043 being conducted?

This trial has 17 study locations across Colorado, District of Columbia, Georgia, Hawaii, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial