Skip to content

Application of recombinant human erythropoietin in the perioperative period of total hip arthroplasty

Application of recombinant human erythropoietin in the perioperative period of total hip arthroplasty

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039970
Enrollment
Unknown
Registered
2020-11-15
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

osteoarthritis, osteonecrosis of femoral head

Interventions

experimental group:The patient was subcutaneously injected with erythropoietin after THA
control group:Nil

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients who were 18 years or older and diagnosed as osteoarthritis or osteonecrosis of femoral head were recruited in this study.

Exclusion criteria

Exclusion criteria: 1) were contraindicated to rHu-EPO; 2) had lower extremity deep venous thrombosis (DVT), pulmonary embolism or myocardial infarction and receive anticoagulant therapy or antiplatelet treatment recently; 3) had severe liver diseases, uncontrolled hypertension, clinically significant impairment of renal function or any other organ insufficiencies; 4) preoperative Hb < 90g/l; 5) had a history of hip fracture or required additional osteotomy during THA.

Design outcomes

Primary

MeasureTime frame
weight;

Secondary

MeasureTime frame
age;height;

Countries

China

Contacts

Public ContactKaijin Guo

Affiliated Hospital of Xuzhou Medical University

kaijinguo@163.com+86 18796283238

Outcome results

None listed

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