Clinical Trials Directory

Trials / Completed

CompletedNCT05393817

Caffeine Citrate Use and Electronic Activity of the Diaphragm (EDI) Changes

Changes in Diaphragmatic Activity Before and After Caffeine Citrate Administration and Discontinuation

Status
Completed
Phase
Study type
Observational
Enrollment
14 (actual)
Sponsor
Seoul St. Mary's Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Caffeine citrate, the first-line agent for apnea of prematurity, enhances diaphragmatic activity. EDI values of neurally adjusted ventilatory assist (NAVA) modes can be used to quantify the diaphragmatic activity triggered by electrical impulse from the respiratory center. This study aims to evaluate the EDI changes following caffeine citrate administration and cessation in preterm infants, and whether such changes are affected by different doses used variably in clinical settings.

Detailed description

Caffeine citrate has been used as the first-line agent for apnea of prematurity. It works via mechanisms including stimulation of the respiratory center in medulla, increasing sensitivity to carbon dioxide retention, and increment in diaphragmatic activity. The effect of caffeine citrate has been evaluated largely based on parameters concerning clinical symptoms (e.g., decrease in the number of apnea, extubation success, decreased incidence of bronchopulmonary dysplasia) but not quantified parameters of actual diaphragmatic activity. Also, while usual doses of caffeine administration is described in the literature, consensus on the effect of caffeine citrate depending on different dosages has not been established. The current study aims to evaluate effect of caffeine citrate by quantifying the electrical impulses of diaphragmatic activity using EDI values captured from neurally adjusted ventilatory assist (NAVA) mode. Out of preterm infants necessitating invasive or non-invasive ventilators, those who are supported by invasive or non-invasive NAVA would be recruited. EDI changes would be monitored for the following timepoints: at the administration of caffeine citrate loading dose, 1st maintenance dose after loading, and at cessation of caffeine citrate.

Conditions

Interventions

TypeNameDescription
DRUGcaffeine citratecaffeine citrate administration, dosage decided by the the physician on duty, within the range of routine management (5mg/kg/day \~ 20mg/kg/day)

Timeline

Start date
2022-06-08
Primary completion
2023-10-18
Completion
2023-10-18
First posted
2022-05-26
Last updated
2023-11-28

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05393817. Inclusion in this directory is not an endorsement.