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A study on the effect of different compression methods on the compression effect of neonates after blood collection

A study on the effect of different compression methods on the compression effect of neonates after blood collection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111718
Enrollment
Unknown
Registered
2025-11-05
Start date
2024-11-12
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Neonatal Blood Collection

Interventions

A group:The cotton ball is pressed manually for 3 minutes
B group:The cotton ball is fixed with tape and pressed for 3 minutes
C group:The cotton ball is fixed with 3M elastic bandage and pressed for 3 minutes
D group:The cotton ball is pressed manually for 4 minutes
E group:The cotton ball is fixed with tape and pressed for 4 minutes
F group:The cotton ball is fixed with 3M elastic bandage and pressed for 4 minutes
G group:The cotton ball is pressed manually for 5 minutes
H group:The cotton ball is fixed with tape and pressed for 5 minutes
I group:The cotton ball is fixed with 3M elastic bandage and pressed for 5 minutes

Sponsors

Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pediatric patients who require blood sampling due to clinical diagnosis and treatment needs; 2. The patient’s guardian voluntarily participates and provides signed informed consent; 3. The blood sampling site is the radial artery; 4. The puncture site has no skin injury or any other ongoing procedures; 5. The puncture is successful on the first attempt.

Exclusion criteria

Exclusion criteria: 1. Pediatric patients discharged, transferred to another department, or deceased within 24 hours of admission; 2. Pediatric patients with congenital malformations, congenital diseases, twin-to-twin transfusion syndrome, coagulation disorders, anemia, thalassemia, polycythemia, Rh hemolytic disease, or other hematologic disorders; 3. Infants with gestational age <28 weeks, or birth weight <1 kg, or Neonatal Critical Illness Score (NCIS) <70; 4. Pediatric patients currently receiving anticoagulation therapy; 5. Infants whose mothers have moderate to severe anemia, thalassemia, polycythemia, Rh hemolytic disease, ABO hemolytic disease, or other hematologic disorders; 6. Pediatric patients whose guardians have declined or partially declined resuscitation or treatment.

Design outcomes

Primary

MeasureTime frame
Success rate of hemostasis;

Secondary

MeasureTime frame
Bleeding of puncture site;Bleeding of subcutaneous tissue;Temperature of hand;Oxygen saturation;Coagulation Indicators in Pediatric Patients;General Information of Pediatric Patients (e.g., gender, gestational age, diagnosis, length of hospital stay, and healthcare costs);

Countries

China

Contacts

Public ContactSu Xi , Yang Yuan

Guangzhou Medical University

282268513@qq.com+86 150 1317 2181

Outcome results

None listed

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