Clinical Trials Directory

Trials / Unknown

UnknownNCT03917394

Erythropoietin And/Or Iron Sucrose For Perioperative Anemia Management In Hip and Knee Arthroplasty

Efficacy and Safety of Erythropoietin And/Or Intravenous Iron Sucrose For Treatment of Anemia In Hip and Knee Arthroplasty: A Single-center Retrospective Study

Status
Unknown
Phase
Study type
Observational
Enrollment
780 (estimated)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Perioperative anemia is very common in patients undergoing total hip arthroplasty (THA) and total knee arthroplasty (TKA). This study retrospectively analyzes the use of rHuEPO and iron sucrose in patients undergoing total hip and knee arthroplasty in order to observe the short-term efficacy and safety of rHuEPO and iron sucrose.

Detailed description

This study aims to explore whether short-term use of rHuEPO and iron sucrose can improve postoperative anemia and promote postoperative rehabilitation after hip and knee arthroplasty. According to different therapies of perioperative anemia , included subjects would be divided into rHuEPO monotherapy group, iron sucrose monotherapy group, rHuEPO combined with iron sucrose group and control group (without rHuEPO and iron sucrose).

Conditions

Interventions

TypeNameDescription
DRUGrHuEPOrHuEPO was administrated daily with 10000 IU or 20000 IU
DRUGIron sucroseIron sucrose was administrated daily with 100mg or 200mg

Timeline

Start date
2019-04-24
Primary completion
2019-05-30
Completion
2019-09-30
First posted
2019-04-17
Last updated
2019-04-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03917394. Inclusion in this directory is not an endorsement.