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Effectiveness of two different strategies of preoperative using recombinant human erythropoietin injection in patients undergoing fast-tract total hip arthroplasty or total knee arthroplasty with anemia

Effectiveness of two different strategies of preoperative using recombinant human erythropoietin injection in patients undergoing fast-tract total hip arthroplasty or total knee arthroplasty with anemia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008227
Enrollment
Unknown
Registered
2016-04-06
Start date
2016-04-07
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

End-staged joint diseases

Interventions

A:basic blood management+EPO preoperative 3 days to postoperative 5 days first time 40000U then 10000U one time*8 days
B:basic blood management+EPO postoperative 5 days, first time 40000U then 10000U one time*5 day

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients receiving total hip arthroplasty/total knee arthroplasty for end-staged joint diseases; 2. Aged from 40-70 years with no limitation of gender; 3. For male, the preoperative Hb should be no more than 130g/L. For female, the preoperative Hb should be no more than 115g/L; 4. Patients who volunteered to participate in clinical trials and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients combined with acute trauma, tumor, severe osteoporosis, other autoimmune diseases and severe muscle contracture deformity around hip/knee; 2. Previous history of neuro-vascular injury, vasculitis and diabetic foot etc; 3. Related thrombosis history, such as pulmonary embolism, thrombosis and deep vein thrombosis in recent three months; 4. Coagulation disorders, bleeding tendency or intraoperative active bleeding; 5. Clear history of iron metabolism disorders; 6. Sever comorbidities in brain cardiovascular system, liver (ALT or AST >2 high limitation of normal value), kidney (BUN >1.5 high limitation of normal value or Cr> 1.5 high limitation of normal value), endocrine, nerve, hematopoietic system or consciousness disorders; 7. Pregnancy or breast-feeding; 8. Allergy to the test drug and human serum albumin, severe allergies, drug or alcohol depedence; 9. Participate in other clinical trials in recent three months; 10. The surgeons believe the patients not suitable for this clinical trial.

Design outcomes

Primary

MeasureTime frame
HB;expenditure;

Secondary

MeasureTime frame
Hit;RET;perioperative transfusion;Transfusion rate;anemia rate;Range of motion;ESR;CRP;IL6;

Countries

China

Contacts

Public ContactZhou Zong-ke

West China Hospital, Sichuan University

zongke@126.com+86 18980601028

Outcome results

None listed

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