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NCT01356927 · ClinicalTrials.gov registry record

Same-day Long-acting Reversible Contraception for Medication Abortion

A clinical trial of Abortion, Induced, sponsored by Boston University.

Completed
Registry status
40
Enrollment target
1
Study location

NCT01356927 is a study of Abortion, Induced that has completed, run by Boston University. The registered enrollment target is 40 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT01356927, a study of Abortion, Induced, has completed, sponsored by Boston University.

COMPLETED
Registry status
40 participants
Enrollment target
1
Study location

Study Summary

Contraception after abortion is an important public health issue, as women who have an abortion are at high risk for additional unintended pregnancy. In the context of first trimester medical abortion, the standard of care is to administer long-acting reversible contraception, including the etonogestrel implant (Implanon) and depot medroxyprogesterone acetate (DMPA), at a follow-up appointment after the abortion. The investigators plan to conduct a prospective observational pilot study to evaluate the satisfaction of subjects who have selected either the contraceptive implant or DMPA given on the first day of medical abortion, as opposed to at a follow-up appointment. The investigators will also assess the continuation of DMPA and Implanon at 3, 6, 9, and 12 months after the initial date of administration. In addition, the investigators will assess the total days of bleeding after the abortion, follow-up rate for evaluation of completion of medical abortion, and efficacy of medical abortion. A total of 40 participants will be recruited, 20 who choose Implanon and 20 who choose DMPA. They will be asked to fill out questionnaires during the course of the study, and will be followed for one year. The study duration including data analysis will be two years.

Conditions Studied

Interventions

  • DRUG DMPA
  • DRUG Etonogestrel implant

Study Locations (1)

Massachusetts

  • Boston University Medical Center - Boston

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2011-05
Est. Completion 2014-04

Sponsor

Boston University

185 total trials

What the Registry Record Tells You About NCT01356927

The ClinicalTrials.gov registry entry for NCT01356927 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston University, which has 185 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Abortion, Induced appearing as the primary indexed condition, and to 2 interventions - of which DMPA is the first listed.

NCT01356927 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01356927 about?

NCT01356927 is a clinical study titled "Same-day Long-acting Reversible Contraception for Medication Abortion". Contraception after abortion is an important public health issue, as women who have an abortion are at high risk for additional unintended pregnancy. In the context of first trimester medical abortion, the standard of care is to administer long-acting reversible contraception, including the etonoges...

What is the current status of trial NCT01356927?

This trial is currently completed. The enrollment target is 40 participants. The study started on 2011-05. Estimated completion is 2014-04.

What conditions does trial NCT01356927 study?

This clinical trial studies the following conditions: Abortion, Induced.

What interventions are being tested in trial NCT01356927?

The interventions under investigation include: DMPA (DRUG), Etonogestrel implant (DRUG).

Who is sponsoring clinical trial NCT01356927?

This trial is sponsored by Boston University, which has 185 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01356927 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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