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Comparison of hemostatic effect of passive pulse pressure patch and sterile dry cotton swabs in needle withdrawal after static pulse puncture

Comparison of hemostatic effect of passive pulse pressure patch and sterile dry cotton swabs in needle withdrawal after static pulse puncture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096239
Enrollment
Unknown
Registered
2025-01-21
Start date
2025-02-09
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

None

Interventions

Experimental group:Venous puncture blood collection using passive pressure pulse hemostatic patch (Chengdu Xin Aoguan Medical Equipment Co., Ltd.) compression hemostasis. Tear the end of the paper-pla
Control group:The use of sterile dry cotton swabs compression hemostasis, before removing the needle to guide the patient or family members to the correct method of pressure, the operation of the nurs

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Those aged 18~80, who are conscious, can correctly express pain and voluntarily participate in this research project were included.

Exclusion criteria

Exclusion criteria: 1. Patients with hematologic diseases; 2. Those with a history of severe allergic reaction or allergic constitution; 3. There is redness, swelling and ulceration at the intravenous injection site; 4. Those who have confusion or expression disorder; 5. Patients with skin allergy to viscose, thin skin and poor nutritional status; 6. Those who resist intravenous injection or compression.

Design outcomes

Primary

MeasureTime frame
Needle bleeding;Subcutaneous congestion;Hematoma;

Secondary

MeasureTime frame
Comfort level;

Countries

China

Contacts

Public ContactLuo Ou

West China Hospital of Sichuan University

luoou1973@163.com+86 136 8904 2890

Outcome results

None listed

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