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
| Type | Name | Description |
|---|---|---|
| DRUG | Mifepristone | Day one of medical abortion |
| DRUG | etonorgestrel |
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.