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Clinical Trials in China / NCT06772272
Active, not recruiting Phase 3

Effect of Perioperative Roxadustat in Elective Lumbar Interbody Fusion Surgery.

NCT06772272 · tracked via the Priya Life Science China tracker
Sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Phase
Phase 3
Started
2024-11-10
Last updated
2025-01-13

Condition(s) studied

Perioperative Anemia

Investigational drug(s) / intervention(s)

Roxadustat →

Roxadustat: Roxadustat is an oral hypoxia-inducible factor prolyl-hydroxylase inhibitor (HIF-PHI) used to treat anemia. Participants in the Roxadustat group will receive 100mg of Roxadustat orally three times per week for three weeks (two weeks prior to surgery and one week post-surgery). The dosage may be adjusted based on hemoglobin levels during the perioperative period: if hemoglobin rises above 150g/L, the drug will be stopped; if hemoglobin increases by more than 20g/L from baseline but is still below 130g/L, the dosage will be reduced to 70mg; if hemoglobin drops by more than 20g/L from baseline, the dosage will be increased to 120mg.

Study summary

The goal of this clinical trial is to assess whether Roxadustat can reduce perioperative blood transfusions in patients with anemia undergoing elective lumbar interbody fusion surgery. It will also evaluate the safety of Roxadustat in this context. The main questions it aims to answer are:

* Does Roxadustat reduce the need for perioperative red blood cell transfusions?
* Is Roxadustat safe for use in patients during the perioperative period?

Researchers will compare Roxadustat to standard clinical care without Roxadustat to determine its effectiveness and safety.

Participants will:

* Take Roxadustat orally three times a week for three weeks (two weeks before surgery and one week post-surgery).
* Undergo regular blood tests and follow-up monitoring during the hospital stay and up to 6 months after surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years, no upper age limit, sex unrestricted. * Scheduled for elective lumbar interbody fusion surgery. * Diagnosed with anemia (Hemoglobin levels: male \<130g/L, female \<120g/L). * Willing to participate and able to voluntarily sign an informed consent form. Exclusion Criteria: * Patients admitted on an emergency basis. * Patients with moderate to severe anemia (Hemoglobin levels \<90g/L). * Patients already enrolled in another clinical study. * Patients unable to comply with the study protocol due to cognitive or language barriers. * Pregnant or breastfeeding women. * Patients who have already received erythropoiesis-stimulating agents, iron supplements, or other treatments to increase hemoglobin levels. * Patients with severe infections. * Patients with a history of acute coronary syndrome, heart failure, or cerebrovascular events within the last 3 months. * Any other medical condition that may pose a safety risk, confound efficacy or safety evaluations, or interfere with study participation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Second Affiliated Hospital of Zhejiang University, School of Medicine Hangzhou Zhejiang

More Second Affiliated Hospital, Zhejiang University, School of Medicine trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06772272 on ClinicalTrials.gov ↗ ← All trials in China