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Asphyxia Neonatorum clinical trials

View clinical trials related to Asphyxia Neonatorum.

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NCT ID: NCT02445417 Completed - Encephalopathy Clinical Trials

Brain Activity During Birth for Prediction of Newborns at Risk for Brain Injury

Start date: June 25, 2015
Phase:
Study type: Observational

The purpose of this study is early identification of asphyxiated newborns through eeg starting in the delivery room.

NCT ID: NCT02347241 Completed - Neonatal Asphyxia Clinical Trials

Infant Special Program for In Hospital Resuscitation Education in the Delivery Room

INSPIRE-D
Start date: January 2014
Phase: N/A
Study type: Interventional

The overall objective is to determine whether a bundled In-hospital Newborn Resuscitation Edu-cation intervention (INSPIRE-D) improves process of care associated with improved newborn survival and neurologic outcomes.

NCT ID: NCT02071160 Completed - Perinatal Asphyxia Clinical Trials

Melatonin for Neuroprotection Following Perinatal Asphyxia

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to examine the effect of combining melatonin to whole body cooling on the brain injury and outcome of neonates following perinatal asphyxia.

NCT ID: NCT02042118 Completed - Asphyxia Neonatorum Clinical Trials

Randomized Clinical Trial Assessing Laryngeal Mask Airway Versus Face-mask Ventilation in Neonatal Resuscitation

LMAvsFMV
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the use of a laryngeal mask airway (LMA) vs. face-mask ventilation (FMV) during first-line neonatal resuscitation in Mulago Hospital, Kampala, Uganda.

NCT ID: NCT02002039 Completed - Perinatal Asphyxia Clinical Trials

Neuroprotective Role of Erythropoietin in Perinatal Asphyxia

Start date: June 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Whether Erythropoietin improves the neurological outcomes of neonates with perinatal asphyxia.

NCT ID: NCT01913340 Completed - Clinical trials for Hypoxic-ischemic Encephalopathy

Neonatal Erythropoietin And Therapeutic Hypothermia Outcomes in Newborn Brain Injury (NEATO)

NEATO
Start date: September 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Hypoxic-ischemic encephalopathy (HIE), a condition of reduced blood and oxygen flow to a baby's brain near the time of birth, may cause death or neurologic disability. Cooling therapy (hypothermia) provides some protection, but about half of affected infants still have a poor outcome. This clinical trial will determine if the drug erythropoietin, given with hypothermia, is safe to use as a treatment that may further reduce the risk of neurologic deficits after HIE.

NCT ID: NCT01869582 Completed - Clinical trials for Respiratory Depression

Safer Births - Reducing Perinatal Mortality

Start date: March 2013
Phase: N/A
Study type: Interventional

Safer Births is a research and development collaboration to establish new knowledge and new innovative products to better equip and increase competence of health workers for safer births and increased newborn survival worldwide. The main objectives are: To randomize different devices for fetal heart rate assessments. To assess if a novel Newborn Resuscitation Monitor will facilitate newborn resuscitation in a low-resource setting. To determine bag mask ventilation treatment and devices beneficial for neonatal outcome.

NCT ID: NCT01866358 Completed - Asphyxia Neonatorum Clinical Trials

Intraosseous Infusion for Neonatal Asphyxiated Resuscitation

Start date: May 2013
Phase: N/A
Study type: Interventional

Intraosseous infusion is better than umbilical vein infusion for neonatal asphyxiated resuscitation

NCT ID: NCT01865656 Completed - Sepsis Clinical Trials

A Skills and Drills Intervention for Emergency Obstetrics and Neonatal Care at First Referral Units of North Karnataka

Start date: July 2013
Phase: N/A
Study type: Interventional

To evaluate the effectiveness of a First Referral Unit (FRU) Emergency Obstetric and Newborn Care (EmONC) skills and drills intervention, to estimate the appropriateness and effectiveness of referrals in intervention arm compared to control arm and to calculate the incremental cost and cost effectiveness of EmONC skills and drills intervention.

NCT ID: NCT01826903 Completed - Depression Clinical Trials

Perinatal Depression Treatment and Child Development

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine whether the successful perinatal depression intervention among mothers (Thinking Healthy Programme, THP) has led to improved developmental outcomes in the children 6 years later. Economic and human resources aspects of the intervention will also be evaluated to determine overall societal benefits from investment in such a program, feasibility of scaling up the intervention and its sustainability in the long-term. The primary hypothesis is that children of mothers who participated in the THP will have better cognitive outcomes and socio-emotional functioning when compared to children of mothers randomized to the control group.