# Pacertool Early Feasibility Study - Safety and Performance

> **NCT06103539** · — · UNKNOWN · sponsor: **Pacertool AS** · enrollment: 50 (estimated)

## Conditions studied

- Heart Failure With Reduced Ejection Fraction
- Dyssynchrony
- Medical Device Performance

## Interventions

- **DEVICE:** Cardiac catheterization and evoked response to cardiac stimulation

## Key facts

- **NCT ID:** NCT06103539
- **Lead sponsor:** Pacertool AS
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2023-12-01
- **Primary completion:** 2024-09-01
- **Final completion:** 2024-12-30
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2023-10-26


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06103539

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06103539, "Pacertool Early Feasibility Study - Safety and Performance". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT06103539. Licensed CC0.

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