Maternal Anemia

2

Review clinical trials related to Maternal Anemia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

MMS, IFA, and MMS+IFA Supplementation in Pregnant Women

This study aims to compare the effectiveness of Multiple Micronutrient Supplementation (MMS), Iron-Folic Acid (IFA) supplementation, and combined MMS+IFA supplementation among pregnant women. Maternal anemia and micronutrient deficiencies are common during pregnancy and can adversely affect both maternal and neonatal health outcomes. A total of 402 pregnant women with gestational age of 20 weeks or less will be randomly assigned to receive MMS, IFA, or combined MMS+IFA supplementation. Participants will be followed throughout pregnancy until delivery. Maternal hemoglobin levels, maternal compliance with supplementation, and neonatal outcomes including birth weight, preterm birth, APGAR scores, and congenital anomalies will be assessed. The findings of this study will provide evidence to guide antenatal nutrition policies and practices in Pakistan.

Participants needed: 402
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Sindh Institute of Child Health and NeonatologyUpdated: Jul 1, 2026
Eligibility criteria

Pregnant women aged 18 years or older [+5]

Severe anemia requiring injectable treatment (hemoglobin <7 g/dL) [+6]

Status: Recruiting

Better Birth Outcomes Through Technology, Education, and Reporting

This is a pragmatic randomized control trial to evaluate the BETTER intervention compared to standard obstetrical care (control) to determine whether it helps to reduce maternal anemia and other adverse pregnancy outcomes. The BETTER intervention includes one motivational interviewing session and bi-weekly text messages to encourage patients to connect with resources that address their social needs, including housing, food, and transportation. Quantitative data will be used to study participant outcomes, including surveys, and electronic health record data.

Participants needed: 550
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Ohio State UniversityUpdated: Jun 9, 2026Locations: 3
Eligibility criteria

Less than 20 weeks and 6 days pregnant upon enrollment [+5]

Has a significant medical condition (eg sickle cell disease) that is a cause of... [+1]