drugset / Trial / NCT02499354

Pilot Study: Randomized, Placebo-controlled Comparator Trial of IV vs Oral Iron Treatment of RLS With IDA. (IVOR-IDA)

NCT02499354

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the study is to determine the relative effect size of standard IV and oral iron treatment of RLS with Iron deficiency anemia (IDA) and to determine the time course of treatment response.

Timeline

Start
2014-08
Primary completion
2021-09-28
Completion
2022-05-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ferrous Sulfate Diagnostic / imaging agent 325 mg Oral
Comparator Iron sucrose Unknown 510 mg Intravenous