Pregnancy and Childbirth
Conditions
Interventions
Provision of Ultrasound services
None
Sponsors
Imaging the World Corp
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: This study will include all pregnant women who will voluntarily consent to participate in the study, between the ages of eighteen- and forty-nine-years attending routine antenatal care or scheduled for an obstetric ultrasound at one of the study sites, and their neonates
Exclusion criteria
Exclusion criteria: The study will exclude: a. All women who do not sign a consent form b. All women on non-routine obstetric ultrasound scan c. All women below eighteen years of age & above fifty or more years of age
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study will have 2 co-primary outcomes: i.Referral of the mother to a higher level of care prior to delivery ii. Location of delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| The study will have several secondary outcomes. These are need for neonatal resuscitation in the form of bag-mask ventilation at delivery, Apgar scores assigned to the neonate following delivery, maternal post-partum hemorrhage, stillbirth, neonatal death up to 28 days post-delivery, maternal death up to 42 days post-delivery. | — |
Countries
Uganda
Contacts
Public ContactDelia Horn
Assistant Professor of Pediatrics
Outcome results
None listed