← Browse by Condition
Medical Condition

respiratory distress syndrome in premature infant

Total Trials
4
Recruiting Now
4
Trial Phases
Various

ClinicalMetric tracks all active clinical trials for respiratory distress syndrome in premature infant sourced from ClinicalTrials.gov. Research in this area spans early-phase safety investigations through large Phase 3 confirmatory trials, conducted by NIH-funded academic centers, independent investigators, and pharmaceutical sponsors worldwide. Each listing is updated daily as new studies open enrollment and existing ones reach capacity or complete follow-up.

Trial listings include the NCT identifier, current recruitment status, phase classification, primary and secondary endpoints, estimated enrollment size, participating countries, and direct links to the full protocol on ClinicalTrials.gov. Eligibility criteria — including age range, disease stage, and prior treatment requirements — are documented for every study to help patients and clinicians assess suitability before contacting a trial site.

Frequently Asked Questions — respiratory distress syndrome in premature infant Clinical Trials

How many clinical trials are currently recruiting for respiratory distress syndrome in premature infant?
ClinicalMetric currently tracks 4 actively recruiting clinical trials for respiratory distress syndrome in premature infant, sourced in real time from ClinicalTrials.gov. The total number of registered studies—including those not yet enrolling or in active follow-up—is 4. Trial availability changes daily as new studies open enrollment and existing ones reach capacity.
What trial phases are available for respiratory distress syndrome in premature infant?
respiratory distress syndrome in premature infant research spans multiple clinical trial phases. Phase 1 studies evaluate safety and dosing in small groups, Phase 2 studies assess preliminary efficacy in 100–300 participants, and Phase 3 trials compare the new treatment against the standard of care in 300–3,000+ patients. Phase 4 post-approval studies monitor long-term outcomes in real-world populations.
How do I find out if I qualify for a respiratory distress syndrome in premature infant clinical trial?
Eligibility criteria for respiratory distress syndrome in premature infant trials vary by study and typically specify age range, disease stage or severity, prior treatment history, and specific diagnostic or laboratory parameters. Each listing on ClinicalMetric links to the full protocol on ClinicalTrials.gov, where inclusion and exclusion criteria are documented. Contact the sponsoring site's research coordinator directly to confirm your eligibility—your treating physician or specialist can also help identify the most appropriate trial based on your medical history and current treatment status.
Top Sponsors
Kafrelsheikh University 1 trial
Rigshospitalet, Denmark 1 trial
University College Dublin 1 trial
Queen Fabiola Children's University Hospital 1 trial

Recruiting Clinical Trials

NCT06642285
Recruiting
Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support
Enrollment
30 pts
Location
Egypt
Sponsor
Kafrelsheikh University
View Trial →
NCT05609877
Recruiting
The NONA-LISA Trial
Enrollment
324 pts
Location
Denmark
Sponsor
Rigshospitalet, Denmark
View Trial →
NCT06557551
Recruiting
Prophylactic Surfactant by Thin Endotracheal Catheter for Preterm Infants At Birth: the ProTeCt Trial
Enrollment
164 pts
Location
Ireland
Sponsor
University College Dublin
View Trial →
NCT06280872
Recruiting
Physiologically Based Cord Clamping To Improve Neonatal Outcomes In Moderate And Late Preterm Newborns
Enrollment
180 pts
Location
Belgium
Sponsor
Queen Fabiola Children's Unive...
View Trial →

Related Conditions

mechanical ventilation complication (1) infant newborn diseases (1) prematurity (1) prematurity extreme (1) premature birth (1) sepsis (1) intraventricular hemorrhage of prematurity (1) bronchodysplasia (1) jaundice (1)
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology