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RECRUITING
NCT06968936
NA

Long-term Outcomes Sub-Study of Preoperative Combined Iron Therapy

Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University

View on ClinicalTrials.gov

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

Interventions

DRUG

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.

PROCEDURE

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