Evaluating the application of LeesCa® Venogram Balloon Catheter for coronary venography, a prospective, multicenter, single-group clinical investigation

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400089647

Enrollment

Unknown

Registered

2024-09-12

Start date

2024-10-01

Completion date

Unknown

Last updated

2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic heart failure

Interventions

Single-arm group:Using LeesCa Venogram Balloon Catheter for coronary venography

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1) Age = 18 2) LeesCa® Venogram Balloon Catheter is planned for coronary venography 3) Sign the informed consent form

Exclusion criteria

Exclusion criteria: 1) Known severe allergy to contrast media 2) Unable to establish an intravenous approach to the right atrium with the interventional device 3) Lactating or pregnant women 4) Not suitable for inclusion in the clinical investigation by the judgment of the investigator

Design outcomes

Primary

Measure	Time frame
Device success rate;	—

Secondary

Measure	Time frame
Acute procedure success rate;Left ventricular lead implantation time;Contrast medium dose;Total X-ray exposure time;Total X-ray exposure dose;	—

Countries

China

Contacts

Public ContactLi Xuebin

Pekiing University People’s Hospital

docxuebin.li@vip.sina.com+86 137 0110 7107

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026