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A prospective randomized controlled study of perioperative application erythropoietin in total knee arthroplasty

A prospective randomized controlled study of perioperative application erythropoietin in total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063117
Enrollment
Unknown
Registered
2022-08-31
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

severe hip/knee diseases

Interventions

EPO group:Using EPO and iron perioperatively
control group:Using iron perioperatively

Sponsors

Joint Surgery, Department of Orthopaedic Medicine, 4th Medical Center, PLAGH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 55-75 years; 2. Knee diseases require total knee replacement; 3. Primary unilateral artificial joint replacement.

Exclusion criteria

Exclusion criteria: 1. Contraindications for EPO use; 2. Contraindications of iron use; 3. Preoperative anemia, less than 120g/L in adult males and less than 110g/L in adult females; 4. Postoperative severe anemia, Hb less than 60g/L; 5. Combined with coagulopathy; 6. Combined with hematopoietic dysfunction; 7. Combined with malignant tumor and other systemic wasting diseases; 8. Combined kidney disease; 9. Previous history of myocardial infarction, pulmonary infarction and cerebral infarction; 10. Robot-assisted joint replacement.

Design outcomes

Primary

MeasureTime frame
Blood routine examination;Absolute reticulocyte count;D-Dimer;Vascular ultrasound of both lower limbs;Thrombelastography;International normalized ratio;Fibrinogen;Activated partial thrombin time;Thrombin activity;Thrombin time;

Countries

China

Contacts

Public ContactChai Wei
chaiweiguanjie@sina.com+86 13601372998

Outcome results

None listed

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