Clinical trial · Observational
Observational Prospective Study on Patients With Symptomatic Uterine Fibroids Treated With VizAblate® Intrauterine-ultrasound Guided RF Ablation
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Investigational device changes
Summary
Brief summary (as posted)
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.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Leiomyoma | Leiomyoma | ONTOLOGY_EXACT | 0.98 |
| Menorrhagia | — | UNRESOLVED | — |
| Uterine Fibroids | Uterine Corpus Leiomyoma | ALIAS | 0.90 |
| Uterine Fibroma | — | UNRESOLVED | — |
| Uterine Neoplasms | Uterine Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| VizAblate System | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- VizAblate treatment
- description
- VizAblate System with subject serving as her own control
- interventionNames
- Device: VizAblate System
Primary outcomes (1)
- measure
- Mean percentage change in treated fibroid perfused volume
- timeFrame
- 12 months
Secondary outcomes (7)
- measure
- Fibroid total volume reduction
- timeFrame
- 12 months
- measure
- Incidence of Intrauterine adhesiogenesis
- timeFrame
- 7 weeks
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 28 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available