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Clinical Study of Radial Artery Compressor

Clinical Study of Radial Artery Compressor

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17010371
Enrollment
Unknown
Registered
2017-01-10
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

transradial intervention, TRI

Interventions

Test team:Use radial artery compressor produced by CHEST company
Control group:Use radial artery compressor produced by other domestic factory

Sponsors

Shanghai Chest Hospital, Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 years; 2. Patient after transradial intervention; 3. Having read the subject's instructions, agreed to enter the group and signed ICF.

Exclusion criteria

Exclusion criteria: 1. Reject to sigh the ICF

Design outcomes

Primary

MeasureTime frame
Hemostatic effect;—

Countries

China

Contacts

Public ContactWang Liang

Shanghai Chest Hospital, Shanghai Jiaotong University

190083871@qq.com+86 18017320205

Outcome results

None listed

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