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A prospective randomized trial on the use of tourniquet in primary total knee arthroplasty

A prospective randomized trial on the use of tourniquet in primary total knee arthroplasty

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034260
Enrollment
Unknown
Registered
2020-06-30
Start date
2015-03-01
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Total knee arthroplasty

Interventions

1:The tourniquet may be inflated before the incision and deflated following confirmed hardening of the cement.
2:Tourniquet be inflated prior to cement application and deflated following hardening
3:Tourniquet be inflated before the initial incision and deflated following completion of skin closure

Sponsors

Queen Mary Hospital, The University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients suffer from primary osteoarthritis indicated for total knee arthroplasty; 2. Subject is physically and mentally willing and able to comply with the postoperative scheduled clinical and radiographic evaluations; 3. Subject must have signed an informed consent document specific to the study, and approved by the Ethics Committee, indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Subject requires a revision knee arthroplasty surgery; 2. Subject is currently on anti-coagulant therapy or has coagulopathy; 3. Subject has peripheral vascular disease of the lower limb evidenced by the presence of blood vessel calcification on the radiographs or the absence of dorsalis pedis/popliteal pulses; 4. Subject suffers from conditions other than primary knee osteoarthritis, e.g. inflammatory arthritis; 5. Subject having associated medical diseases affecting rehabilitation; 6. Subject has active systemic infection or infection near the knee joint; 7. Subject having current medical condition that render them unfit for surgery; 8. Any criteria which in the opinion of the investigator, suggests that the subject would not be compliant with the study protocol.

Design outcomes

Primary

MeasureTime frame
The peri-operative blood loss and muscle damage;

Secondary

MeasureTime frame
Post-operative thigh pain and bruise, knee range of motion, muscle power;

Countries

China

Contacts

Public ContactChun-Hoi Yan

Department of Orthopaedics & Traumatology, Queen Mary Hospital

yanchunhoi@gmail.com+852 92595159

Outcome results

None listed

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