# A Prospective Cohort Study to Evaluate the Safety, Efficacy, and Usability of the EpiZact Device

> **NCT06729255** · PHASE4 · NOT_YET_RECRUITING · sponsor: **Oregon Health and Science University** · enrollment: 100 (estimated)

## Conditions studied

- Postdural Puncture Headache
- Epidural Analgesia, Obstetric

## Interventions

- **DEVICE:** EpiZact-assisted epidural placement

## Key facts

- **NCT ID:** NCT06729255
- **Lead sponsor:** Oregon Health and Science University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2025-03-15
- **Primary completion:** 2026-03-15
- **Final completion:** 2026-12-31
- **Target enrollment:** 100 (ESTIMATED)
- **Last updated:** 2025-02-14

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06729255

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06729255, "A Prospective Cohort Study to Evaluate the Safety, Efficacy, and Usability of the EpiZact Device". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06729255. Licensed CC0.

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