# Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids

> **NCT05386615** · — · RECRUITING · sponsor: **InSightec** · enrollment: 200 (estimated)

## Conditions studied

- Uterine Fibroid

## Interventions

- **DEVICE:** Body System - Functional

## Key facts

- **NCT ID:** NCT05386615
- **Lead sponsor:** InSightec
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2016-02-16
- **Primary completion:** 2026-12-31
- **Final completion:** 2026-12-31
- **Target enrollment:** 200 (ESTIMATED)
- **Last updated:** 2025-04-30


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05386615

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05386615, "Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids". Retrieved via AI Analytics 2026-06-14 from https://api.ai-analytics.org/clinical/NCT05386615. Licensed CC0.

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