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Effect of Different Compression Durations on the Incidence of Vascular Complications at the Femoral Artery Puncture Site After Neurointervention

Effect of Different Compression Durations on the Incidence of Vascular Complications at the Femoral Artery Puncture Site After Neurointervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125348
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-06-02
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

cerebrovascular disease

Interventions

Group A:The compression device was released after 4 hours of compression, followed by 6 hours of immobilization of the puncture-side limb.
Group B:The compression device was released after 6 hours of compression, followed by 8 hours of immobilization of the puncture-side limb.
Group C:The compression device was released after 8 hours of compression, followed by 10 hours of immobilization of the puncture-side limb.

Sponsors

Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years, both genders included; 2. Stable vital signs (blood pressure 90–160/60–100 mmHg, heart rate 60–120 beats per minute); 3. Undergoing diagnostic cerebral DSA angiography or uncomplicated neurointerventional therapeutic procedures; 4. The patient or their legally authorized representative has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Women who are pregnant or breastfeeding; 2. Combined with severe primary diseases of the liver, kidney, cardiovascular system, or hematopoietic system; 3. Presence of impaired consciousness or mental illness that prevents cooperation with postoperative immobilization; 4. Long-term use of two or more antiplatelet agents or anticoagulants; 5. Unsuccessful puncture procedure (e.g., repeated punctures =3 times, inadvertent puncture of the femoral vein, etc.); 6. Known coagulation abnormalities (PLT 1.5, PT > 1.2 times the normal value, or APTT > 1.5 times the normal value); 7. Severe obesity (BMI = 35 kg/m²); 8. Previous surgery or scar tissue at the puncture site.

Design outcomes

Primary

MeasureTime frame
Local hematoma;Active hemorrhage;Arteriovenous fistula;Pseudoaneurysm;Retroperitoneal hematoma;

Secondary

MeasureTime frame
Pain;Comfort level;Sleep quality;Dysuria / Urinary retention;

Countries

China

Contacts

Public ContactQiyong Mei

Changzheng Hospital

meiqiyong@smmu.edu.cn+86 159 0083 0439

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026