Infant Death

9

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

Condition / disease
Location
Status: Recruiting

Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries- PreTerm

The goal of this multicenter, cluster-randomized, crossover trial is to determine if umbilical cord milking compared to early cord clamping will reduce in-hospital mortality in non-vigorous preterm infants born between 30 weeks and 34 weeks of gestation.

Participants needed: 800
Trial details
Age: 0-10Biological sex: AllType: InterventionalSponsor: Nemours Children's ClinicUpdated: Jul 13, 2026Locations: 9
Eligibility criteria

Preterm infants born between 30 0/7 weeks to 34 6/7 weeks of gestation [+1]

Infants with congenital malformation [+6]

Status: Recruiting

Advanced Wireless Sensors for Neonatal Care in the Delivery Room

The goals of this observational study is to assess whether a new advanced wireless skin sensor vital sign monitoring system can effectively monitor the vital signs of healthy newborn infants (≥ 35 weeks gestational age). The main aims of this Study are to: 1. Assess feasibility 2. Evaluate safety 3. Determine accuracy of the wireless monitoring system, compared to the standard of care wired vital sign monitoring system, immediately after delivery and for the first 2h of age in the obstetrical center under unsupervised parents' care. The newborn infants participating in the Study will have both vital sign monitoring systems placed on their chest and limb. Their vital signs will be monitored for 2h consecutively.

Participants needed: 600
Trial details
Age: 35-42Biological sex: AllType: InterventionalSponsor: Guilherme Sant'Anna, MDUpdated: May 8, 2026Locations: 5
Eligibility criteria

Newborns ≥35 weeks (gestational age) [+2]

Newborns ≤ 35 weeks (gestational age) [+2]

Status: Not yet recruiting

Walk With Me (WWM) for Perinatal Grief

The goal of this clinical trial is to learn if the Along With Me web-based intervention works to decrease posttraumatic stress symptoms and suicidal ideation among bereaved parents following pregnancy and early infant loss. It will also learn whether peer guides provide additional improvements on these outcomes. The main questions it aims to answer are: • Do people who receive Along With Me or Along With Me plus a Peer Guide compared to services as usual have lower posttraumatic stress symptoms and suicidal ideation than those who do not receive the intervention? Researchers will compare Along With Me and Along With Me plus a Peer Guide to services as usual (referrals made in the hospital setting) to see if Along With Me works to prevent and address posttraumatic stress symptoms and suicidal ideation. Participants will: * Receive access to a mobile app with approximately 10 therapeutic modules about how to manage grief and other symptoms. * Receive check-ins with a Peer Guide (in the Peer Guide condition only)

Participants needed: 300
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: Oregon Research Behavioral Intervention Strategies, Inc.Updated: Mar 6, 2026Locations: 1
Eligibility criteria

Within the first month of pregnancy or early infant loss [+3]

Not pregnant or has not experienced an early infant loss [+3]

Status: Not yet recruiting

Determining the Effect of Midwife-Led Safe Infant Care Training for Pregnant Women on Awareness of Sudden Infant Death Syndrome and Home Accidents

This project is a pioneering study in determining the impact of midwife-led safe infant care training for pregnant women on awareness of sudden infant death syndrome (SIDS) and home accidents. Raising awareness and improving women's knowledge about SIDS and home accidents is expected to help reduce preventable infant deaths. If the effectiveness of this training is proven, integrating it into prenatal care programs would be a significant step towards improving maternal and child health.

Participants needed: 120
Trial details
Biological sex: FemaleType: InterventionalSponsor: Cukurova UniversityUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

Volunteering to participate in the research [+3]

Diagnosed high-risk pregnancy [+2]

Status: Recruiting

Support Via Online Social Networks to Promote Safe Infant Care Practices

This study aims to improve adherence to American Academy of Pediatrics safe sleep (SS) recommendations and improve rates of initiation and duration of partial and exclusive breastfeeding (BF); and reduce Black/White disparities in these practices through the use of private Facebook groups providing a) evidence-based education through videos and other multi-media supporting best practices and b) an online community and social network of other pregnant WIC clients and new parents.

Participants needed: 3,000
Trial details
Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Jan 12, 2026Locations: 1
Eligibility criteria

Currently enrolled in WIC, or it not, then have either Medicaid or no health ins... [+4]

Not planning to live in same home as infant after birth. [+5]

Status: Recruiting

The Happiest Baby, Inc. SNOO Postmarket Surveillance Study

This postmarket surveillance study will evaluate the safety of the SNOO Smart Sleeper Bassinet when used for infants who are at high risk for Sudden Unexpected Infant Death (SUID). This study will survey 1000 caregivers of high-risk infants to examine the frequency of death or serious injury occurring in the SNOO Bassinet.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Happiest Baby, Inc.Updated: Sep 5, 2025Locations: 1
Eligibility criteria

Respondent must identify as a primary caregiver of the infant. [+9]

Not primary caregiver [+10]

Status: Recruiting

Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries- PreTerm

The goal of this multicenter, cluster-randomized, crossover trial is to determine if umbilical cord milking compared to early cord clamping will reduce in-hospital mortality in non-vigorous preterm infants born between 30 weeks and 34 weeks of gestation.

Participants needed: 800
Trial details
Age: 0-10Biological sex: AllType: InterventionalSponsor: Nemours Children's ClinicUpdated: Jul 11, 2025Locations: 9
Eligibility criteria

Preterm infants born between 30 0/7 weeks to 34 6/7 weeks of gestation [+1]

Infants with congenital malformation [+6]

Status: Recruiting

Get Social Media and Risk-Reduction Training

This study examines the implementation of the TodaysBaby™ mobile safe sleep intervention program in US hospitals. The main aims of this study are to examine: 1) differences in program penetration and the equity of penetration according to income and race/ethnicity; 2) differences in feasibility, acceptability, sustainability and fidelity top the intervention; and 3) the effectiveness of the intervention.

Participants needed: 10,000
Trial details
Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Jun 11, 2025Locations: 1
Eligibility criteria

Must speak English or Spanish [+4]

A prenatal diagnosis expected to have impact on infant care practices not compat...

Status: Recruiting

Increasing Neonatal HIV Test and Treat to Maximize the Long-Term Impact on Infant Health and Novel Infant Antiretroviral Treatment

This study aims to improve HIV healthcare services for mothers living with HIV and their newborns in Tanzania and Mozambique. The main questions it aims to answer are: 1) does enhancing screening with maternal HIV viral load monitoring at delivery identify more mother-child pairs at high-risk for HIV vertical transmission? and 2) are high-risk infants linked to appropriate prevention and care? The study will expand access to HIV testing services to more rural settings using a hub-and-spoke referral system.

Participants needed: 6,000
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Michael HoelscherUpdated: Nov 18, 2024Locations: 2
Eligibility criteria

Voluntary and informed consent of the mother for her own study participation (if... [+5]

Deficiency in the mother, rendering it difficult, if not impossible, for her or... [+7]