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NCT04710342: CapBuster

Clinical Study Evaluating Use of the CapBuster Medical Device System for the Crossing of Chronic Total Occlusions

Status unknown NA Last updated 21 February 2023
What this trial tests

NA trial testing CapBuster in Chronic Total Occlusion in 26 participants. Status unknown.

Timeline
21 June 2021
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorPraxis Medical Devices Ltd
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment26
Start date21 June 2021
Primary completion31 December 2023
Estimated completion31 December 2023
Sites1 location across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Praxis Medical Devices Ltd

Who can join

18 and older, any sex, with Chronic Total Occlusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study represents a prospective, non-randomized, dual-center clinical study to evaluate the safety and effectiveness of the CapBuster System in crossing a de novo or restenotic infrapopliteal chronic total occlusion. Measures of safety and efficacy will be assessed through 30 days post-intervention.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Chronic Total Occlusion

Currently open trials in the same condition.

Other Praxis Medical Devices 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/NCT04710342.

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