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Pregnancy Outcome in Women With an Iron Deficiency in the First Trimester

University Hospital Basel logo

University Hospital Basel

Status

Completed

Conditions

Iron Deficiency

Treatments

Other: Data collection (laboratory and obstetric results)

Study type

Observational

Funder types

Other

Identifiers

NCT05262634
2020-02033 bb22Hoesli2;

Details and patient eligibility

About

The primary aim of this retrospective, monocentric study with two parallel groups is to investigate pregnancy outcome in women with iron deficiency in the first trimester. It compares the pregnancy outcome between pregnant women with an iron deficiency and those without an iron deficiency in the first trimester. The study group are pregnant women with a diagnosed iron deficiency in the first trimester, a total of 227 pregnant women. The control group consists of 486 pregnant women without first-trimester iron deficiency. Matching criteria include parity and maternal age. Data from patient files of pregnant women who were treated in the Women's Clinic, University Hospital Basel between 2017 and 2019 are analyzed.

Enrollment

713 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant women with a documented iron deficiency in the first trimester
  • Pregnant women with normal hematological parameters and iron status in the first trimester
  • Treated at the Women's Clinic, University Hospital in Basel

Exclusion criteria

  • Pregnant women with a documented rejection

Trial design

713 participants in 2 patient groups

study group: iron deficiency
Description:
Pregnant women with a documented iron deficiency in the first trimester
Treatment:
Other: Data collection (laboratory and obstetric results)
control group: normal iron status
Description:
Pregnant women with normal hematological parameters and iron status in the first trimester
Treatment:
Other: Data collection (laboratory and obstetric results)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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