ClinicalTrials.gg
RecruitingNCT06061393Updated Sep 11, 2026

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

A Phase 4 interventional study of Venofer 200 MG Per 10 ML Injection and Ferinject in Anemia, Iron Deficiency and Pregnancy Anemia, sponsored by Western Galilee Hospital-Nahariya. Recruiting at 1 site in Israel. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-09-11.

Sponsored by Western Galilee Hospital-Nahariya · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Started Nov 2023; still recruiting 3 years later.
Phase
Phase 4
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Female
01

Study summary

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.

02

Conditions studied

  • Anemia, Iron Deficiency
  • Pregnancy Anemia
03

In context

Anemia, Iron-Deficiency

600 studies on the registry are indexed under Anemia, Iron-Deficiency; 95 are open to participants now.

This study's planned enrollment of 200 is above the median of 100 across 459 interventional studies indexed under Anemia, Iron-Deficiency.

Browse Anemia, Iron-Deficiency studies →

Lead sponsor

Western Galilee Hospital-Nahariya is the lead sponsor of 89 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

pregnancy>24 weeks of gestation anemia with \<9 anemia with Hb\<9.5 if symptomatic anemia or previous postpartum hemorrhage

Exclusion criteria

Exclusion Criteria:

  • Allergy to one of the study's drugs
  • IV iron treatment in the last month
  • Underlying medical conditions associated with anemia, such as thalassemia Major, renal insufficiency, or spherocytosis
  • Twin pregnancy
  • non iron deficiency anemia
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Active comparator
    venofer

    Women with iron def. anemia aith hemoglobin level \<9 gr/dl who will be traeted with venofer

    Drug: Venofer 200 MG Per 10 ML Injection

  • Active comparator
    Ferinject

    Women with iron def. anemia aith hemoglobin level \<9 gr/dl who will be traeted with ferinject

    Drug: Ferinject

Interventions

06

What researchers measure

Primary outcomes

  1. ratio of women with Hb level >11 at delivery

    Hb level

    Time frame: at delivery

  2. postpartum Hb level

    gr/dl

    Time frame: during 48 hours after delivery

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2023 (actual). Primary completion is estimated for Sep 2027, 46 months after the start.

Of 43 non-industry phase 4 interventional studies under Anemia, Iron-Deficiency, half reached primary completion within 20 months of starting (the median), counting those still running; a quarter within 14 and three quarters within 35. This study's planned 46 months is above that.

Counting every sponsor, half of 51 studies reached it within 22 months; a quarter within 15 and three quarters within 35.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 24, 2023
First posted
Sep 29, 2023
StartActual
Nov 2, 2023
Primary completionEst.
Sep 2027
CompletionEst.
Dec 2027
Last update
Sep 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06061393
Lead sponsor
Western Galilee Hospital-Nahariya
Responsible party
Dr. Maya Wolf (Principal Investigator., Western Galilee Hospital-Nahariya) — Principal investigator
First posted
Sep 29, 2023
Start date
Nov 2, 2023
Primary completion
Sep 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Sep 11, 2026

Study contacts

maya Wolf, MD
Contact
mayaw@gmc.gov.il
972507887800

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Iron sucrose · Ferric carboxymaltose

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