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Comparison Between Outcomes of Pregnant Women Treated With Ferinject vs. Venofer for Iron Deficiency Anemia

W

Western Galilee Hospital-Nahariya

Status and phase

Not yet enrolling
Phase 4

Conditions

Anemia, Iron Deficiency
Pregnancy Anemia

Treatments

Drug: Venofer 200 MG Per 10 ML Injection
Drug: Ferinject

Study type

Interventional

Funder types

Other

Identifiers

NCT06061393
0120-23-NHR

Details and patient eligibility

About

The purpose of this study is to compare maternal outcomes such as increased hemoglobin need for blood transfusion and hemoglobin level before and post partum in women with hemoglobin <9 gr/dl , treated with venofer and women treated with ferinject.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

pregnancy>24 weeks of gestation anemia with Hb<8 anemia with Hb<9 if symptomatic anemia of previous postpartum hemorrhage

Exclusion criteria

  • Allergy to one of the study's drugs
  • IV iron treatment in the last month
  • chronic anemia- thalassemia, renal failure Twins pregnancy
  • non iron deficiency anemia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

venofer
Active Comparator group
Description:
Women with iron def. anemia aith hemoglobin level \<9 gr/dl who will be traeted with venofer
Treatment:
Drug: Venofer 200 MG Per 10 ML Injection
Ferinject
Active Comparator group
Description:
Women with iron def. anemia aith hemoglobin level \<9 gr/dl who will be traeted with ferinject
Treatment:
Drug: Ferinject

Trial contacts and locations

0

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Central trial contact

maya Wolf, MD

Data sourced from clinicaltrials.gov

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