Immediate vs. Delayed Insertion of Copper T 380A IUD After Termination of Pregnancy Over 12-weeks Gestation

Completed · Not applicable

Conditions studied: Contraception Behavior

In brief

The purpose of this study is to compare delayed vs. immediate insertion of the Copper T 380 IUD after termination of pregnancy after 12 weeks.

Key facts

Study ID

NCT00540046

Run by

NYU Langone Health

People needed

215

Starts

2007-04-01

Expected to finish

2010-02-01

Last updated by the study team

2015-02-09

Who can join

Age: 16 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• women 16 years of age and older
• intrauterine pregnancy > 14 weeks gestation
• desires termination of pregnancy
• desires IUD for contraception
• ability to give informed consent
• no contraindication for D+E

You may not qualify if…

• unable to give informed consent
• less than 16 years of age
• congenital or acquired uterine anomaly including fibroids if they distort the uterine cavity
• acute pelvic inflammatory disease (PID)
• known or suspected uterine or cervical neoplasia or unresolved abnormal PAP smear
• untreated acute cervicitis or vaginitis, until infection treated/controlled
• confirmed Chlamydia trachomatis or Neisseria gonorrhea infection in the previous 90 days
• acute liver disease or liver tumor (benign or malignant)
• woman or partner currently with multiple sexual partners
• history of Wilson's disease
• hypersensitivity to any component of Copper T IUD

Where it is running

• Bellevue Hospital — New York, New York, United States
• Parkmed Women's Clinic — New York, New York, United States

Full record on ClinicalTrials.gov

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