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Disposable Radial Artery Compression Hemostatic Device Clinical Study Protocol

Disposable Radial Artery Compression Hemostatic Device Clinical Study Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108635
Enrollment
Unknown
Registered
2025-09-02
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Patients requiring temporary compression hemostasis at the radial artery puncture site

Interventions

Intervention group:Compression hemostasis using Single-Use Radial Artery Compression Hemostat (Model: ZXQ-A1111)

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Subjects who need to stop bleeding with temporary compression of the radial artery puncture; 2. 18 years old< = age< = 80 years old; 3. Allen test positive; 4. Subjects who sign the informed consent form and can cooperate with the entire trial process.

Exclusion criteria

Exclusion criteria: 1. Chronic kidney disease; 2. Cirrhosis; 3. Radial artery development malformation; 4. Those with coagulation dysfunction; 5. The researcher believes that there is any situation that is not suitable for selection.

Design outcomes

Primary

MeasureTime frame
Hemostasis Success Rate;

Secondary

MeasureTime frame
Hematoma Formation;Hemostasis Time (min);Hand Pain/Swelling;Other Adverse Events;Bleeding Grade;Puncture Site Inflammation;

Countries

China

Contacts

Public ContactXiaoping Zhu

Shanghai Tenth People's Hospital

juliya1107@163.com+86 21 66301604

Outcome results

None listed

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