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Trials / Completed

CompletedNCT02037919

Nexplanon Application Post-Abortion (NAPA)

Immediate vs. Delayed Insertion of Nexplanon After Termination of Pregnancy Over 14-weeks Gestation (NAPA)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
148 (actual)
Sponsor
Family Planning Associates Medical Group, LTD · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Women who receive Nexplanon immediately post abortion will be significantly more likely to be using the device 6 months after the procedure than those assigned to receive the device 2-4 weeks after the procedure.

Detailed description

Women will be contacted 6 months after their abortion to ask about contraception use and side effects.

Conditions

Interventions

TypeNameDescription
OTHERImmediate Nexplanon InsertionPatient will have a Nexplanon inserted within 15 minutes of her abortion
OTHERPost-op Nexplanon InsertionPlace Nexplanon at post operative visit rather than at surgery

Timeline

Start date
2014-06-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2014-01-16
Last updated
2024-02-12
Results posted
2024-02-12

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02037919. Inclusion in this directory is not an endorsement.

Nexplanon Application Post-Abortion (NAPA) (NCT02037919) · Clinical Trials Directory