Evaluation of ContraMed VeraCept Intrauterine Copper Contraceptive for Long Acting Reversible Contraception

1. Between 18-40 years of age at the time of study initiation; 1.1 Enrollment will be targeted for 225 subjects aged 18-35 (for safety and effectiveness analyses) and an additional 25 subjects aged 36-40 (for safety only) (note: all subjects will be included in the analysis for device placement and tolerability);

2. Pre-menopausal, as determined by regular menstrual cycle (28 ± 5 days) for the last 3 months; 2.1 Based on patient history, when not on hormonal contraceptives;

3. Sexually active with a male partner who has not had a vasectomy;

4. Reasonably expect to have to coitus at least once monthly during the study period.

5. Married or in a steady relationship (e.g., 3-6 months);

6. Seeking to avoid pregnancy for the next 12 months;

7. Willing to use the study device as the sole form of contraception;

8. Willing to accept a risk of pregnancy;

9. Normal PAP or ASC-US with negative high risk HPV test result within the appropriate screen timeframe, unless considered at risk;

10. Able and willing to comply with all study tests, procedures, assessment tools and follow-up; and

11. Able and willing to provide and document informed consent and Authorization for Release of Protected Health Information (PHI).

1. Known or suspected pregnancy; or at risk for pregnancy from unprotected intercourse earlier in current cycle

2. Subject who anticipates separation from her partner for more than 1 cycle within the next 12 months;

3. A previously inserted IUD that has not been removed by the time VeraCept is placed;History of previous IUD complications, such as perforation, expulsion, infection (pelvic inflammatory disease) or pregnancy with IUD in place;

4. History of previous serious IUD complications;

5. Injection of hormonal contraceptive (e.g., Depo-Provera) within the last 10 months; 6.1 Must have had 2 normal menstrual cycles since the last injection;

6. Planned use of any non-contraceptive estrogen, progesterone or testosterone any time during the 12 months of study participation;

7. Postpartum, prior to a minimum of 6 weeks or complete uterine involution;

8. Exclusively breastfeeding before return of menses; Lactating women will be excluded unless they have had have had two normal menstrual periods. 8.1 Must have had 2 normal spontaneous menstrual cycles since delivery

9. Unexplained abnormal uterine bleeding (suspicious for serious condition), before evaluation; Immediately post-septic abortion or puerperal sepsis;

10. Severely heavy or painful menstrual bleeding;

11. Suspected or known cervical, uterine or ovarian cancer, or unresolved clinically significant abnormal pap smear requiring evaluation or treatment Any history of gestational trophoblastic disease with or without detectable elevated ß-hCG levels, or related malignant disease;

12. Known anatomical abnormalities of the uterine cavity that may complicate IUD placement, such as: 12.1 Submucosal uterine leiomyoma 12.2 Asherman's syndrome 12.3 Pedunculated polyps 12.4 Bicornuate uterus 12.5 Didelphus or uterine septa

13. Known anatomical abnormalities of the cervix such as severe cervical stenosis, prior trachelectomy or extensive conization that, in the opinion of the investigator would prevent cervical dilation and study device placement;

14. Current or recent (within the last 3 months) pelvic infection (cervix, endometrium, or fallopian tubes), or mucopurulent cervicitis;

15. High risk for STDs (e.g., multiple sexual partners);

16. Known or suspected AIDS;

17. Known intolerance or allergy to nickel or copper, including Wilson's Disease;

18. Currently participating or planning future participation in a research study of an investigational drug or device during the course of this investigational study;

19. Subject had VeraCept placed previously or had 2 attempts at placement;

20. Known or suspected alcohol or drug abuse within 12 months prior to the screening visit;

21. Any general health or behavioral condition that, in the opinion of the Investigator, could represent an increased risk for the subject or would render the subject less likely to provide the needed study information.