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Long-term Outcomes Sub-Study of Preoperative Combined Iron Therapy
Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University
Summary
This is a sub-study of the Preoperative Combined Iron Therapy trail in which some participants will be additionally randomized to combined iron supplementation or standarded treatment control to evaluate the impact on long-term outcomes.
Official title: Long-term Outcomes Sub-Study of Preoperative Combined Iron Therapy in Anemic Patients Undergoing Cardiac Surgery: A Randomized Controlled Trial
Key Details
Gender
All
Age Range
18 Years - 85 Years
Study Type
INTERVENTIONAL
Enrollment
400
Start Date
2026-03-27
Completion Date
2029-06-30
Last Updated
2026-04-13
Healthy Volunteers
No
Conditions
Interventions
Sucrose Iron,subcutaneous recombinant human erythropoietin,intravenous vitamin C
Patients in the experimental group will receive a combination therapy consisting of intravenous sucrose iron (200 mg), subcutaneous recombinant human erythropoietin (150 IU/kg), and intravenous vitamin C (2 g), administered once daily for three consecutive days within the week prior to surgery.
Routine perioperative management
Routine perioperative management based on clinical judgment, including observation, monitoring, and standard nursing practices.
Locations (1)
Department of Anesthesiology, Second Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, China