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NCT06103539

Pacertool Early Feasibility Study - Safety and Performance

Status unknown Last updated 26 October 2023
What this trial tests

trial testing Cardiac catheterization and evoked response to cardiac stimulation in Heart Failure With Reduced Ejection Fraction in 50 participants. Status unknown.

Timeline
1 December 2023
Primary endpoint
1 September 2024
30 December 2024

Quick facts

Lead sponsorPacertool AS
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date1 December 2023
Primary completion1 September 2024
Estimated completion30 December 2024
Sites1 location across Georgia

Drugs / interventions tested

Conditions studied

Sponsor

Pacertool AS

Who can join

Adults 18 to 80, any sex, with Heart Failure With Reduced Ejection Fraction or Dyssynchrony. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study is a non-randomized, two-part, open label, prospective single-site, single arm, safety and performance study. The study is designed to collect acute and long-term clinical data and user reported outcome data from using the PreSens-Catheter and PACER Software during cardiac catheterization and Cardiac Resynchronization Therapy (CRT) device implantation procedures. Subjects with indication for arterial catheterization and CRT will be included.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Heart Failure With Reduced Ejection Fraction

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06103539.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing