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Effect of SUPER patency hemostasis in radial artery patency hemostasis: a randomized controlled trial

Effect of SUPER patency hemostasis in radial artery patency hemostasis: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095203
Enrollment
Unknown
Registered
2025-01-03
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

radial artery occlusion

Interventions

Standard patency hemostasis:“SUPER” Patent Hemostasis Method
Standard patency hemostasis:Standard patency hemostasis

Sponsors

Nanjing Lishui Peolpe's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Age = 18 years and < 80 years; 2.Patients undergoing coronary angiography in the cardiology department; 3.Patients with clear consciousness, understanding and expression ability; 4.Patients who are willing to participate in the study and provide written informed consent; 5.Antiplatelet drug use: aspirin enteric-coated tablet 300mg+ ticagrelor tablet 180mg/ Clopidogrel bisulfate tablet 300mg one day before surgery; On the day of surgery, aspirin enteric-coated tablet 100mg+ ticagrelor tablet 90mg/ Clopidogrel bisulfate tablet 75mg;

Exclusion criteria

Exclusion criteria: 1.Patients with upper limb disability or deformity; 2.Patients with local skin or tissue edema or infection; 3.Patients with coagulation dysfunction or severe comorbidities who have had two or more ipsilateral radial artery punctures; 4.The puncture point is not 1-2cm below the metacarpal stripe;

Design outcomes

Primary

MeasureTime frame
Incidence of 24-hour RAO;

Secondary

MeasureTime frame
Incidence of vascular complications;Bleeding complication rate;convenience;

Countries

China

Contacts

Public ContactDunfu Zhang

Nanjing Lishui Peolpe's Hospital

1334698493@qq.com+86 18795929518

Outcome results

None listed

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