Clinical Trials Directory

Trials / Completed

CompletedNCT01920022

Quickstart of Nexplanon® at Medical Abortion

Early Versus Delayed Insertion of Nexplanon® at Medical Abortion - a Randomized Controlled Equivalence Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
551 (actual)
Sponsor
Karolinska Institutet · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Women having abortions are at high risk for subsequent unintended pregnancy and repeat abortion. Clearly, encouraging contraceptive use after abortion is a high priority. Long acting reversible contraceptives (LARCs, Implants and intrauterine contraception) are the most effective methods to help women avoid a repeat unwanted pregnancy and abortion. Studies in surgical abortion patients, show that "quickstart" of a LARC - i.e., inserting it during the surgical procedure - is associated with substantially greater use of that method six months later than requiring women to return later to get the device. However, today a majority of women chose medical abortion. The clinical routine is to insert LARCs at the follow up 2 to 3 weeks after the abortion treatment. Frequently women choose to do part of the abortion treatment at home and do not return for a follow up. Thus, the possibility to quick start a contraceptive method in medical abortion would be a major advantage especially if this could be done at the time of administration of mifepristone.

Conditions

Interventions

TypeNameDescription
DRUGMifepristoneDay one of medical abortion
DRUGetonorgestrel

Timeline

Start date
2013-10-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2013-08-09
Last updated
2016-02-25

Locations

7 sites across 2 countries: Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT01920022. Inclusion in this directory is not an endorsement.