# Pre-Post Intervention Study to Investigate the Safety, Feasibility, & Efficacy of the NeurGear ZenBud System for the Treatment of Anxiety & Anxiety-Related Symptoms

> **NCT06574971** · NA · ACTIVE_NOT_RECRUITING · sponsor: **NeurGear** · enrollment: 30 (estimated)

## Conditions studied

- Anxiety Disorders

## Interventions

- **DEVICE:** Low intensity focused ultrasound using the NeurGear Zenbud

## Key facts

- **NCT ID:** NCT06574971
- **Lead sponsor:** NeurGear
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2024-08-15
- **Primary completion:** 2024-10-15
- **Final completion:** 2025-08-15
- **Target enrollment:** 30 (ESTIMATED)
- **Last updated:** 2024-08-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06574971

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06574971, "Pre-Post Intervention Study to Investigate the Safety, Feasibility, & Efficacy of the NeurGear ZenBud System for the Treatment of Anxiety & Anxiety-Related Symptoms". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT06574971. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*