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Clinical Observation of the Patent-Converted Product "Disposable Radial Artery Compression Hemostatic Device" Following Transarterial Coronary Interventional Procedures

Clinical Observation of the Patent-Converted Product "Disposable Radial Artery Compression Hemostatic Device" Following Transarterial Coronary Interventional Procedures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102838
Enrollment
Unknown
Registered
2025-05-20
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Radial Artery Puncture Site Injury

Interventions

Control group:NA
Group A:Shorten Compression Duration
Group B:Shorten Compression Duration
Group C:Utilize the disposable radial artery compression hemostatic device and shorten compression duration.

Sponsors

First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged over 18 years undergoing initial coronary interventional procedure; (2) Right radial artery as access site with palpable pulse, positive Allen's test, and hemodynamic stability; (3) Patients conscious with clear comprehension and communication abilities; (4) No restricted mobility in the right upper limb; (5) Signed informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients undergoing emergency surgery; (2) Failed right radial artery interventional procedure; (3) Presence of skin breakdown or scarring at the wrist joint; (4) History of wrist joint fracture; (5) Clinician-assessed high bleeding risk.

Design outcomes

Primary

MeasureTime frame
Hemostasis Rate;Radial Artery Occlusion Rate;

Secondary

MeasureTime frame
Postoperative-Preoperative Difference in Circumference of the Thumb Interp;Patient Comfort;

Countries

China

Contacts

Public ContactQin Gang

First Hospital of Shanxi Medical University

qgsdyy@163.com+86 138 3414 3738

Outcome results

None listed

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