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

Launched by GYNESONICS · Nov 25, 2013

Keywords

ClinConnect Summary

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 approxi...

Gender

FEMALE

Eligibility criteria

• 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