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Clinical Study of Intermittent Hypoxia Reduction Using PIMUN: Efficacy Proof-of-Concept

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 1 month
Healthy Volunteers: t
View:

• Preterm infants with a gestational age at birth \<34 weeks

• Age \<30 days at the time of enrollment

• Documented diagnosis of apnea of prematurity (AOP)

Locations
Other Locations
Chile
Clinica San Carlos de Apoquindo
ACTIVE_NOT_RECRUITING
Santiago
UC Christus Clinical Hospital
RECRUITING
Santiago
Contact Information
Primary
Paulina A Toso, MD
ptoso@med.puc.cl
56223543349
Backup
Alvaro J González, MD
alvgonza@med.puc.cl
56223543224
Time Frame
Start Date: 2024-09-01
Estimated Completion Date: 2026-05-31
Participants
Target number of participants: 20
Treatments
Active_comparator: PIMUN
48 hours of dorsal stimulation by PIMUN. Continous cardiorespiratory monitorization- Brain NIRS first 24 hours- 4-5 hours of Polysomnogram at the second day. Blood and urine samples at the finish.
Sham_comparator: 48 hours without PIMUN
48 hours without PIMUN. Continous cardiorespiratory monitorization- Brain NIRS first 24 hours- 4-5 hours of Polysomnogram at the second day. Blood and urine samples at the finish.
Related Therapeutic Areas
Sponsors
Collaborators: Agencia Nacional de Investigación y Desarrollo
Leads: Pontificia Universidad Catolica de Chile

This content was sourced from clinicaltrials.gov