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Tourniquet versus no tourniquet on rehabilitation after fast-track total knee arthroplasty

Tourniquet versus no tourniquet on rehabilitation after fast-track total knee arthroplasty

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-16008794
Enrollment
Unknown
Registered
2016-07-06
Start date
2015-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Osteoarthritis of knee

Interventions

Treatment group:Receive a tourniquet-assisted knee arthroplasty
Control group:Undergo knee arthroplasty without extended tourniquet use

Sponsors

Department of Orthopaedics, Xijing Hospital, the Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Adult patients who plan to undergo primary TKA on simultaneous bilateral knee joints with a diagnosis of osteoarthritis, but not of rheumatoid arthritis.

Exclusion criteria

Exclusion criteria: 1. Aged >50 or 35 kg/m2; 3. Rheumatoid arthritis; 4. Current chronic anticoagulation therapy; 5. Abnormal coagulation function; 6. Local or systematic infection; 7. Severe deformity of the knee: >20 degree varus or ectropion, >30 degree flexion contracture; 8. Previous open-knee surgery; 9. Diseases of the blood system, cerebral infarction, cerebral hemorrhage, active malignancy; 10. Peripheral vascular or nerve disease; 11. Preoperative anemia (a hemoglobin value of <100 g/L); 12. Surgery not by project surgeon; 13. Patients refused to participate in the study; 14. Psychiatric illness.

Design outcomes

Primary

MeasureTime frame
Quadriceps strength(pre-operation and everyday after the surgery);Knee VAS score after TKA(pre-operation and everyday after the surgery);

Secondary

MeasureTime frame
Postoperative knee flexion(pre-operation and everyday after the surgery);Postoperative limb swelling;Amount of bleeding during operation;Postoperative draining quantity;Patient satisfaction;

Countries

China

Contacts

Public ContactQingsheng Zhu

Department of Orthopaedics, Xijing Hospital, The Fourth Military Medical University

zhuqsh@fmmu.edu.cn+86 029 84775280

Outcome results

None listed

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