Effects of Iron Therapy in Heart Failure With Preserved Ejection Fraction and Iron Deficiency (PREFER-HF)

PHASE3CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

August 23, 2017

Primary Completion Date

September 15, 2024

Study Completion Date

December 20, 2024

Conditions
Heart Failure With Normal Ejection FractionFerropenic Anemia
Interventions
OTHER

Placebo

The group assigned to placebo will receive an infusion of normal saline solution plus oral lactose capsules identical to oral medication.

DRUG

Ferric carboxymaltose

The group assigned to receive intravenous iron will receive intravenous ferric carboxymaltose ajusted by weight and Hb levels according to study protocol plus oral placebo

DRUG

Ferroglycine Sulfate

One group assigned to receive oral iron will receive two 100 mg oral capsule of ferroglycine sulfate plus intravenous placebo (normal saline solution)

DRUG

Sucrosomial Iron

One group assigned to receive oral iron will receive or two oral capsule containing 30 mg of pyrophosphate sucrosomial iron plus intravenous placebo (normal saline solution)

Trial Locations (2)

Unknown

Hospital Universitari Arnau de Vilanova, Lleida

Hospital de Manises, Manises

All Listed Sponsors
collaborator

Fundació La Marató de TV3

OTHER

lead

Institut de Recerca Biomèdica de Lleida

OTHER

NCT03833336 - Effects of Iron Therapy in Heart Failure With Preserved Ejection Fraction and Iron Deficiency (PREFER-HF) | Biotech Hunter | Biotech Hunter