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NCT04862559

A Single Center Study to Evaluate the Safety of the NovaCross Microcatheter in Crossing Chronic Total Occlusions

Completed NA Last updated 28 April 2021
What this trial tests

NA trial testing NovaCross in Chronic Total Occlusion in 15 participants. Completed in 17 September 2017.

Timeline
1 February 2017
Primary endpoint
17 September 2017
17 September 2017

Quick facts

Lead sponsorNitiloop Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date1 February 2017
Primary completion17 September 2017
Estimated completion17 September 2017
Sites1 location across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Nitiloop Ltd.

Who can join

Adults 25 to 80, any sex, with Chronic Total Occlusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an open label, single-center, prospective, pivotal study in which the investigational device, NovaCross™ micro-catheter, will be tested in up to 15 patients scheduled to undergo CTO-PCI using an anterograde approach.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of NovaCross

Trials testing the same drug.

Other recruiting trials for Chronic Total Occlusion

Currently open trials in the same condition.

Other Nitiloop Ltd. trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04862559.

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