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Influence of femoral correlative factors on perioperative blood loss in total hip arthroplasty

Influence of femoral correlative factors on perioperative blood loss in total hip arthroplasty

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046491
Enrollment
Unknown
Registered
2021-05-16
Start date
2021-05-25
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

End stage hip disease

Interventions

Group A:Bone wax closes the medullary cavity
Group B:Bone wax is not used intraoperatively

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients requiring primary total hip arthroplasty due to severe hip osteoarthritis, femoral head necrosis, and secondary osteoarthritis due to developmental hip dysplasia; 2. Aged between 20 and 80 years; 3. Body mass index is between 18.5 and 29.9 kg/m2; 4. The American Society of Anesthesiologists (American Society of Anesthesiologists, ASA) classification (anesthesia risk assessment) I to III levels; 5. Preoperative blood routine and blood coagulation function were normal

Exclusion criteria

Exclusion criteria: 1. Allergic to bone wax and tranexamic acid; 2. Previous thrombosis events, cardiovascular or cerebrovascular history, coagulation dysfunction, and severe liver and kidney dysfunction; 3. History of hip injury and infection; 4. Receiving anticoagulant therapy.

Design outcomes

Primary

MeasureTime frame
Blood loss;

Countries

China

Contacts

Public ContactKang Pengde

West China Hospital, Sichuan University

kangpd@163.com+86 18280213153

Outcome results

None listed

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