drugset / Trial / NCT05913414

Iron Isomaltide for Iron-deficiency Anemia Patients With Locally Advanced Nasopharyngeal Carcinoma

NCT05913414

Phase 2 Unknown 120 enrolled Sun Yat-sen University
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary purpose: To evaluate the difference of hematopoietic response rate at 1 month after concurrent chemoradiotherapy between iron isomaltide and oral iron supplement for treating iron-deficiency anemia patients with locally advanced nasopharyngeal carcinoma. Secondary purpose: To evaluate the difference of hematopoietic response rate, tolerance, acute side effects, qualtiy of life at 2 months and 3 months after concurrent chemoradiotherapy between Iron Isomaltide and oral iron supplement for treating iron-deficiency anemia patients with locally advanced nasopharyngeal carcinoma.

Timeline

Start
2023-05-05
Primary completion
2024-05-30
Completion
2026-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron isomaltoside 1000 Unknown
Comparator Polysaccharide Iron Complex Pill Unknown