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A comparative study for the prevention of deep venous thrombosis in total knee arthroplasty with single and combined preventive strategies

A comparative study for the prevention of deep venous thrombosis in total knee arthroplasty with single and combined preventive strategies

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025672
Enrollment
Unknown
Registered
2019-09-04
Start date
2019-09-03
Completion date
Unknown
Last updated
2019-09-09

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

Conditions

gonarthrosis

Interventions

1:Single prevention strategy
2:Joint prevention strategy

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) male and female patients aged > 50 years old; (2) the patient planned to undergo selective initial artificial knee replacement, with no limitation on either side; (3) preoperative color doppler suggested DVT of both lower limbs (--); (4) no previous history of thromboembolic venereal diseases; (5) the patient volunteered and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) preoperative color doppler examination of DVT (+) in both lower limbs; (2) significant risk factors or active bleeding; (3) coagulation dysfunction; (4) previous history of thromboembolic disease; (5) obvious liver diseases (such as chronic hepatitis, cirrhosis, liver abscess); (6) previous knee revision surgery history; (7) drug or alcohol abusers.

Design outcomes

Primary

MeasureTime frame
Preoperative and postoperative hemoglobin content;blood platelet count;prothrombin time;Activation of partial thrombin time;D-dimer;liver function;Postoperative color doppler examination of both lower limbs was performed;Postoperative blood loss;

Countries

China

Contacts

Public ContactFeng Shuo

Affiliated Hospital of Xuzhou Medical University

781733181@qq.com+86 18552880088

Outcome results

None listed

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