# A Clinical Study to Evaluate Safety of the ExAblate 2100 UF V2 System in the Treatment of Symptomatic Uterine Fibroids

> **NCT01092988** · NA · COMPLETED · sponsor: **InSightec** · enrollment: 40 (estimated)

## Conditions studied

- Uterine Fibroids
- Bleeding
- Pain

## Interventions

- **DEVICE:** Exablate 2100

## Key facts

- **NCT ID:** NCT01092988
- **Lead sponsor:** InSightec
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2010-03
- **Primary completion:** 2012-02
- **Final completion:** 2012-02
- **Target enrollment:** 40 (ESTIMATED)
- **Last updated:** 2012-02-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01092988

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01092988, "A Clinical Study to Evaluate Safety of the ExAblate 2100 UF V2 System in the Treatment of Symptomatic Uterine Fibroids". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT01092988. Licensed CC0.

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