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Completed

NCT Number: NCT03591640

The Validity of Kleinhauer Betke in Women With Known Hemoglobinopathy for Fetal-maternal Hemorrhage

The aim of this study is to determine the validity of Kleinhauer Betke in women with known hemoglobinopathy for fetal-maternal hemorrhage.

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Key information

Conditions

Fetal-Maternal Hemorrhage Anemia Anemia, Neonatal Congenital, Hereditary, and Neonatal Diseases and Abnormalities Fetomaternal Transfusion Hematologic Diseases Hemic and Lymphatic Diseases Infant, Newborn, Diseases

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hille Yaffe Medical Center

Hadera, 38100, Israel

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant with singleton fetus
  • Gestational age 34-42
  • With or without known hemoglobinopathy

Exclusion criteria

  • Known risk factor for fetal maternal hemorrhage

Treatment and study plan

Blood test

Diagnostic Test

Standard blood test

Primary outcomes

  1. Validity of Kleinhauer Betke test in Pregnant Women

    Time frame: 24 hours

    Comparison of Kleinhauer Betke results with electrophoresis results to determine presence of F-hemoglobin. This would indicate the validity of the Kleinhauer Betke test in women with hemoglobinopathy

Sponsors and collaborators

Lead sponsor

Hillel Yaffe Medical Center

Other Gov

Registry information

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Jul 19, 2018
Registry last updated
Jun 28, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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