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Comparison of different intervention methods to reduce the incidence of VTE

Comparison of different intervention methods to reduce the incidence of VTE

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027659
Enrollment
Unknown
Registered
2019-11-23
Start date
2019-12-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Venous thromboembolic

Interventions

Group 1:FRAXIPARINE
Group 2:Enoxaparin Sodium Injection
Group 3:intermittent pneumatic compression device+FRAXIPARINE
Group 4:intermittent pneumatic compression device+Enoxaparin Sodium Injection
Group 5 (control group):Nil

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Aged more than 18 years old; vital signs are stable; Caprini score scale > 2

Exclusion criteria

Exclusion criteria: Open injury can not complete the lower extremities ultrasound examination; vital signs are unstable; Caprini score scale 0-2 points; pregnant and lactating women; intermittent pneumatic compression device cannot be used due to injury site or surgical operation; With anticoagulant contraindications; Have participated in other clinical trials or have participated in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss;30-day mortality;Whether venous thrombosis occurs;—

Countries

China

Contacts

Public ContactWeiFeng Huang

Shanghai Sixth People's Hospital

breeze_huang@sohu.com+86 18930173670

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026