Adiana Post-Approval Clinical Study
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 169
- 试验地点
- 9
- 主要终点
- Pregnancy Rate - for Women Informed They May Rely on the Adiana System for Contraception.
研究概览
简要总结
The Adiana Post-Approval Clinical Study (APACS) has been designed to compile information on the efficacy and safety of the Adiana Permanent Contraception System in the post market setting. Specifically, data will be collected that is relevant to the evaluation of the safety and efficacy of the Adiana System for women who desire permanent birth control by occlusion of the fallopian tubes. This study is an observational study that is not intended to test specific hypotheses.
详细描述
Adiana Post-Approval Clinical Study is a prospective, single armed, multi-center, observational study that is designed to provide additional efficacy and safety data regarding the FDA-approved Adiana Permanent Contraception System. This study will be conducted at 8-10 clinical sites and enroll 1000 subjects. Enrolled subjects will have baseline data collected at the time of their Adiana procedure and will then be followed for a period of 2 years with visits occurring at 3 months following the Adiana procedure, 6 months following Adiana procedure (as applicable), 12 and 24 months post relying date.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Subjects who are seeking permanent sterilization
- •Women 18-45 years old
- •Subjects who are at risk of becoming pregnant
- •Subjects willing to use alternative contraception for at least three (3) months following device placement and bilateral tubal occlusion is confirmed by HSG
- •Subjects who are able to provide informed consent
排除标准
- •Subjects who are uncertain about their desire to end fertility
- •Clinical evidence of an active pelvic infection or history of a recent pelvic infection
- •Has intra-uterine pathology which would prevent access to either tubal ostium or the intramural portion of either fallopian tube (i.e., large submucous fibroids, uterine adhesions, apparent uni or bilateral proximal tubal occlusion, suspected unicornuate uterus, etc.)
- •Is pregnant (as evidenced by pregnancy test result) or suspects pregnancy
- •Is currently less than three (3) months since her last pregnancy
- •Has previously undergone a tubal ligation
- •Is currently taking immunosuppressive medication (e.g., steroids)
- •Has a known allergy to contrast media
- •Has external pacemaker or internal cardioverter defibrillator
- •Subject is unable to follow the protocol and return for follow up visits
- •In the opinion of the investigator, the subject has a medical condition that precludes safe participation in the study
结局指标
主要结局
Pregnancy Rate - for Women Informed They May Rely on the Adiana System for Contraception.
时间窗: At one and two years
The primary efficacy endpoints are the one and two year pregnancy rates among women who have hysterosalpingogram (HSG)-proven bilateral occlusion and are informed that they may rely on the Adiana System for contraception.
次要结局
- Safety Endpoints(At one and two years)