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NCT Number: NCT06554522

Pragmatic Evaluation of Respiratory Distress Syndrome Treatment in Africa

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.

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Key information

Age range

1 hour–24 hour

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Centre Hospitalier Universitaire Communautaire, Bangui, Central African Republic

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Surfactant

Drug

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

Other names: Less Invasive Surfactant Administration Technique

Primary outcomes

  1. Hospital Survival

    Time frame: Through hospitalization, an average of 6 months

    Survival to hospital discharge

Secondary outcomes

  1. Incidence of major preterm neonatal morbidity

    Time frame: Through hospitalization, an average of 6 months

    Intraventricular hemorrhage, Retinopathy of Prematurity, Bronchopulmonary Dysplasia, Surgical Necrotizing Enterocolitis and Culture Positive Sepsis

  2. The incidence of pneumothorax

    Time frame: Through hospitalization, an average of 6 months

    Air leaks into the space between your lung and chest wall

  3. Hospital survival at seven day

    Time frame: 7 days following birth

    Survival rates assessed at day seven of life

Study contacts

Contact information is provided by the study sponsor or research team.

Osayame A Ekhaguere

CONTACT

[email protected]

+13179443691

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Collaborators

  • Coefficient Giving (Formerly Open Philanthropy)

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Aug 15, 2024
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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