Observational Prospective Study on Patients With Symptomatic Uterine Fibroids Treated With VizAblate® Intrauterine-ultrasound Guided RF Ablation

Gynesonics

Status: Terminated

Conditions: Uterine Neoplasms; Uterine Fibroids; Leiomyoma; Uterine Fibroma; Menorrhagia

Treatments: Device: VizAblate System

Study type: Observational

Funder types: Industry

Identifiers

NCT01998854

CL03537

Details and patient eligibility

About

Study is intended to evaluate the one-year safety and clinical status of patients treated for symptomatic uterine fibroids with the VizAblate Intrauterine-ultrasound guided radio frequency (RF) ablation system. Particular attention will be directed to recording safety outcomes including incidence of uterine cavity synechiae. In addition, information on quality of life will be collected.

Overall study duration (first patient enrolled through last patient exit) will be comprised of approximately 12 months of patient enrollment up to 1 month for scheduling of treatment, and 12 months of follow-up, for a total duration of up to 25 months. Study duration for an individual patient, once enrolled, will be approximately 1 month for baseline observations and treatment scheduling, and 12 months for follow up after treatment for a total duration of approximately 13 months.

Full description

In this single-arm study, subjects who receive transcervical intrauterine-ultrasound guided RF ablation of symptomatic uterine fibroids with the VizAblate® System will be assessed with 3D pelvic sonography with contrast, hysteroscopy, and quality of life questionnaires.

Overall study duration (first patient enrolled through last patient exit) will be comprised of approximately 12 months of patient enrollment up to 1 month for scheduling of treatment, and 12 months of follow-up, for a total duration of up to 25 months. Study duration for an individual patient, once enrolled, will be approximately 1 month for baseline observations and treatment scheduling, and 12 months for follow up after treatment for a total duration of approximately 13 months.

Enrollment: 4 patients

Sex: Female

Ages: 28+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 28 years of age or older
• Indication for transcervical treatment of uterine fibroids associated with menorrhagia
• Willingness to participate in the study, to attend all follow-up visits and undergo all study assessments, and to sign the informed consent form
• Presence of submucosal and/or intramural fibroids

Exclusion criteria

• Pregnancy
• ≥40 years of age with desire for current or future fertility, unless the estimated risk/benefit ratio has been determined to be more favorable to future pregnancy than standard therapy
• Non-sterilized patients < 40 years of age, unless the estimated risk/benefit ratio has been determined to be more favorable to future pregnancy than standard therapy
• Active pelvic infection, known or suspected gynecologic malignancy or premalignant condition
• Presence of tubal implant for sterilization
• Previous pelvic irradiation
• Endometrial cavity length, including endocervical canal, < 4.5 cm
• Any abnormality of the vagina or uterine cavity that, in the judgment of the investigator obstructs access of the VizAblate handpiece to the endometrial cavity
• Presence of cardiac pacemaker or other active implant
• Post-menopausal

Trial design

4 participants in 1 patient group

VizAblate treatment

Description:

VizAblate System with subject serving as her own control

Treatment:

Device: VizAblate System