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Pragmatic Evaluation of Respiratory Distress Syndrome Treatment in Africa

Pragmatic Evaluation of Therapies to Enhance Respiratory Management in Preterm Infants in Africa

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06554522
Enrollment
1512
Registered
2024-08-15
Start date
2025-01-01
Completion date
2027-12-30
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature Birth, RDS of Prematurity, Respiratory Distress Syndrome in Premature Infant, Surfactant Deficiency Syndrome Neonatal

Brief summary

The goal of this pragmatic clinical trial is to learn if the drug surfactant given by a less invasive technique works to treat respiratory distress in preterm infants in low- and middle-income African countries where invasive ventilators are unavailable. It will also learn about the safety of the less invasive surfactant administration (LISA) technique. The main questions it aims to answer are: Does surfactant given by a less invasive surfactant administration technique improve survival in preterm infants in low- and middle-income countries? What medical problems do participants have when receiving surfactant given by the less invasive surfactant administration technique? Researchers will implement the less invasive surfactant administration technique and see if it works to treat respiratory distress in preterm infants compared to preterm who did not receive surfactant. Participants with respiratory distress who are being treated with continuous positive airway pressure and caffeine citrate will: Receive surfactant replacement therapy by the less invasive surfactant administration technique. Be monitored for complications Be followed throughout their hospitalization to determine their survival rate.

Detailed description

The low- and middle-income countries of Sub-Saharan Africa (SSA) carry the highest burden of preterm births and deaths. A primary driver of preterm mortality in SSA is respiratory distress syndrome. Surfactant replacement therapy by the less invasive surfactant administration (LISA) is a technique where the surfactant is administered to a preterm neonate with respiratory distress syndrome managed on continuous positive airway pressure (CPAP), reducing the need for using an invasive mechanical ventilator. In high-income countries, LISA has been shown to be effective in reducing the need for invasive mechanical ventilators and mortality. However, the impact of LISA is unknown in low-resourced settings without ventilators. The central hypothesis is that implementing LISA in newborn units that care for preterm neonates using standardized CPAP and caffeine citrate will improve survival in preterm neonates. PICO Outline: Population: Preterm neonates 750 and 2000 grams or gestational age between 24- and 35 weeks at birth with respiratory distress defined by a Silverman Anderson Score of ≥5, who are spontaneously breathing and on CPAP. Intervention: Surfactant administered through the less invasive surfactant administration (LISA), technique. Comparator: Standard of care - standardized CPAP and Caffeine. Outcome measures: Primary Outcome: All-cause in-hospital survival.

Interventions

DRUGSurfactant

Surfactant is instilled into the lungs through a thin catheter passed into the trachea during laryngoscopy while on continuous positive airway pressure (CPAP)

Sponsors

Indiana University
Lead SponsorOTHER
Coefficient Giving (Formerly Open Philanthropy)
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A stepped wedge cluster randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
1 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* Birth weight between 750 and 2000 grams or gestational age between 24- and 35 weeks. * Silverman Anderson Score ≥5 before or after CPAP treatment. * Admitted to a study site within 24 hours of life.

Exclusion criteria

* Major congenital or genetic anomalies. * Active pulmonary hemorrhage. * Major craniofacial anomalies that preclude the successful use of CPAP

Design outcomes

Primary

MeasureTime frameDescription
Hospital SurvivalThrough hospitalization, an average of 6 monthsSurvival to hospital discharge

Secondary

MeasureTime frameDescription
Incidence of major preterm neonatal morbidityThrough hospitalization, an average of 6 monthsIntraventricular hemorrhage, Retinopathy of Prematurity, Bronchopulmonary Dysplasia, Surgical Necrotizing Enterocolitis and Culture Positive Sepsis
The incidence of pneumothoraxThrough hospitalization, an average of 6 monthsAir leaks into the space between your lung and chest wall
Hospital survival at seven day7 days following birthSurvival rates assessed at day seven of life

Countries

Central African Republic, Ghana, Kenya, Nigeria

Contacts

CONTACTOsayame A Ekhaguere
osaekhag@iu.edu+13179443691
PRINCIPAL_INVESTIGATOROsayame A Ekhaguere, MBBS, MPH

Indiana University

PRINCIPAL_INVESTIGATORHelen Nabwera, BMedSci

Aga Khan University

PRINCIPAL_INVESTIGATOROlufunke Bolaji, MBBS

Afe Babalola University

PRINCIPAL_INVESTIGATOREdgardo Szyld, MD, MS

Indiana University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026