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Study identifier: NCT07396103 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy of PIMUN by Reducing Intermittent Hypoxia Events

Condition: Preterm · Apnea of Prematurity · Hypoxemia  ·  Sponsor: Pontificia Universidad Catolica de Chile

PhaseNA
Planned participants20
Who can joinAll sexes, N/A to 30 Days
Healthy volunteersYes

About this study

The goal of this clinical trial is to learn if the use of PIMUN(medical device) works to reduce the intermittent hypoxemia of 24-34 weeks of birth gestational age babies. . It will also learn about the safety of the use of PIMUN. The main questions it aims to answer are: Does PIMUN lower the time of oxygen saturation under 90%? What medical problems do participants have using PIMUN? Researchers will compare the use of PIMUN during 48 hours to 48 hours of usual treatments (not using PIMUN). Participants will: Use/ or not use of PIMUN for a 48 hours period- randomly assigned. Regional brain oxygenation by near infrared spectroscopy (NIRS) monitoring at the first day of each 48 hours period. 4-6 hours of polysomnography at the second day of each intervention. Plasma and urine stress oxygen metabolites at the end of each 48-hours intervention.

This description comes directly from the study's public registry record.

Talk to the study team

Paulina A Toso, MD  ·  56223543349  ·  ptoso@med.puc.cl

Alvaro J González, MD  ·  56223543224  ·  alvgonza@med.puc.cl

Always discuss trial participation with your own doctor first.

Locations (2)

Clinica San Carlos de ApoquindoSantiago, Santiago Metropolitan, ChileActive Not Recruiting
UC Christus Clinical HospitalSantiago, Santiago Metropolitan, ChileRecruiting

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Source record: clinicaltrials.gov/study/NCT07396103