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A Clinical Trial Evaluating the BeneVision V200 Patient Monitor with CRT Module for Monitoring in Pediatric and Adult Populations

A Clinical Trial Evaluating the BeneVision V200 Patient Monitor with CRT Module for Monitoring in Pediatric and Adult Populations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122291
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-10
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

None

Interventions

Manual Reading Group:Actively use the CRT tooling for multiple measurements
Device Group:Measure CRT using the tested device

Sponsors

Shenzhen Bao'an People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 14 years, regardless of gender. 2.The subject or their legal guardian must understand the clinical trial, voluntarily agree to participate, and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1.Inability to wear the CRT sensor. 2.Deemed by the clinician to be unsuitable for participation in this clinical trial.

Design outcomes

Primary

MeasureTime frame
CRTt,j;—

Secondary

MeasureTime frame
CRTr,j;—

Countries

China

Contacts

Public ContactYuehui Zhang

Shenzhen Bao'an People's Hospital

yuehuizhang1645@email.szu.edu.cn+86 755 27788311

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026