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临床试验/CTRI/2022/10/046632
CTRI/2022/10/046632招募中未知

Prevention of Iron Deficiency Anemia Post-delivery (PRIORITY Trial): A Randomized Controlled Trial of the Global Network for Womens and Childrens Health Research - PRIORITy

Eunice Kennedy Shriver National Institute of Child Health and Human Development0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Established pregnancy >20 wk gestation by LMP and/or clinical assessment
  • 2. Confirmed moderate anemia (Hb 7.0 to 9.9 g/dL, 6-48 hr after delivery based on a venous blood sample)
  • 3. Deliver in participating study hospital or health facility
  • 4. Able to provide informed consent
  • 5. Plans to remain in study area for duration of the study

排除标准

  • 1. Contraindication to iron supplementation
  • 2. Blood transfusion already received or scheduled
  • 3. Known diagnosis of pre-existing depression or other psychiatric illness
  • 4. Stillbirth, major congenital anomaly, or neonatal loss prior to facility discharge
  • 5. Women testing positive and previously untreated for malaria
  • 6. Presenting with symptomatic anemia with dyspnea or fatigue and need for immediate correction
  • 7. Women with known hemoglobinopathy (sickle cell disease or thalassemia)
  • 8. Presence of severe allergic conditions such as severe asthma or known drug allergies
  • 9. Women presenting with any illness/condition requiring immediate medical care per physicianâ??s assessment

研究者

发起方
Eunice Kennedy Shriver National Institute of Child Health and Human Development

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