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Exploration of the application of pneumatic pressure device during the period of anticoagulation after artificial knee joint replacement

Exploration of the application of pneumatic pressure device during the period of anticoagulation after artificial knee joint replacement

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049226
Enrollment
Unknown
Registered
2021-07-27
Start date
2020-05-30
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

muscular calf vein thrombosis

Interventions

The experimental group:treated with IPC on both lower extremities within 14h after surgery
The control group:using IPC in both lower limbs immediately after surgery until the first time when they got out of bed.

Sponsors

Department of orthopedics, the second affiliated hospital of the army medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Primary unilateral TKA of the medial parapatellar approach; 2. Volunteered to participate in the experiment and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Preoperative DVT of lower limbs, pulmonary embolism, or thrombophlebitis; 2. Severe arteriosclerosis or stenosis of lower extremity vessels, other ischemic vascular diseases (diabetes, etc.) and severe deformity of lower extremity; 3. Recent active bleeding and coagulation dysfunction; 4. Local abnormalities of lower extremities that are not suitable for IPC (such as dermatitis, gangrene, recent skin grafting); 5. Congestive heart failure, pulmonary edema, or severe edema of the lower limbs; 6. A history of DVT/PE and a family history of thrombotic disease; 7. Heparin-induced thrombocytopenia; 8. Patients with malignant tumor; 9. Patients with other types of hereditary or acquired thrombotic disorder.

Design outcomes

Primary

MeasureTime frame
Incidence of MCVT after surgery;

Countries

China

Contacts

Public ContactZhang Yumei

Department of orthopedics, The Second Affiliated Hospital of Army Medical University

578013843@qq.com+86 15922521737

Outcome results

None listed

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