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

Completed · Phase 2

Conditions studied: Contraception

In brief

Prospective, multi-center, single-arm, open-label, Phase II clinical study to evaluate the effectiveness, device placement, safety, and tolerability of VeraCept to support commencing a Phase III Clinical Study

Key facts

Study ID

NCT02446821

Run by

Sebela Women's Health Inc.

People needed

286

Starts

2015-06-01

Expected to finish

2019-03-22

Last updated by the study team

2026-03-03

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Between 18-40 years of age at the time of study initiation;
• 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);
• Pre-menopausal, as determined by regular menstrual cycle (28 ± 5 days) for the last 3 months;
• 1 Based on patient history, when not on hormonal contraceptives;
• Sexually active with a male partner who has not had a vasectomy;
• Reasonably expect to have to coitus at least once monthly during the study period.
• Married or in a steady relationship (e.g., 3-6 months);
• Seeking to avoid pregnancy for the next 12 months;
• Willing to use the study device as the sole form of contraception;
• Willing to accept a risk of pregnancy;
• Normal PAP or ASC-US with negative high risk HPV test result within the appropriate screen timeframe, unless considered at risk;
• Able and willing to comply with all study tests, procedures, assessment tools and follow-up; and
• Able and willing to provide and document informed consent and Authorization for Release of Protected Health Information (PHI).

You may not qualify if…

• Known or suspected pregnancy; or at risk for pregnancy from unprotected intercourse earlier in current cycle
• Subject who anticipates separation from her partner for more than 1 cycle within the next 12 months;
• 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;
• Injection of hormonal contraceptive (e.g., Depo-Provera) within the last 10 months;
• 1 Must have had 2 normal menstrual cycles since the last injection;
• Planned use of any non-contraceptive estrogen, progesterone or testosterone any time during the 12 months of study participation;
• Postpartum, prior to a minimum of 6 weeks or complete uterine involution;
• Exclusively breastfeeding before return of menses; Lactating women will be excluded unless they have had two normal menstrual periods.
• 1 Must have had 2 normal spontaneous menstrual cycles since delivery
• Unexplained abnormal uterine bleeding (suspicious for serious condition), before evaluation; Immediately post-septic abortion or puerperal sepsis;
• Severely heavy or painful menstrual bleeding;
• 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;
• Known anatomical abnormalities of the uterine cavity that may complicate IUD placement, such as:
• 1 Submucosal uterine leiomyoma
• 2 Asherman's syndrome
• 3 Pedunculated polyps
• 4 Bicornuate uterus
• 5 Didelphus or uterine septa
• 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;
• Current or recent (within the last 3 months) pelvic infection (cervix, endometrium, or fallopian tubes), or mucopurulent cervicitis;
• High risk for STDs (e.g., multiple sexual partners);
• Known or suspected AIDS;
• Known intolerance or allergy to nickel or copper, including Wilson's Disease;

Where it is running

• Essential Access Health (formerly California Family Health Council) — Burbank, California, United States
• Essential Access Health (formerly California Family Health Council) — Los Angeles, California, United States
• University of California Davis Health System — Sacramento, California, United States
• University of Colorado — Aurora, Colorado, United States
• Healthcare Clinical Data, Inc — Miami, Florida, United States
• Columbia University Medical Center — New York, New York, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• Oregon Health and Sciences University — Portland, Oregon, United States
• Clinical Research of Philadelphia — Philadelphia, Pennsylvania, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States
• Advanced Research Associates — Corpus Christi, Texas, United States
• University of Utah — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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