Analysis of the hands-on medical treatment process of preterm apnea
Recruiting
- Conditions
- apnea of prematurity
- Registration Number
- DRKS00018085
- Lead Sponsor
- ni Leipzig Haptik-Labor
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Premature infants < 1500 g birth weight;
Non-invasive breathing aid or no breathing aid;
Postnatal age 0-6 weeks;
gestational age < 32 weeks;
Informing the legal guardians and consent of both legal guardians to the child’s participation in the study, including data collection and storage
Exclusion Criteria
Serious illness, such as sepsis;
Mechanical invasive ventilation;
Chromosomal abnormalities;
Malformations that require surgical correction
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method a) SpO2 during and after different interventions and treatment strategies of the medical staff; b) Duration of hypoxemic episodes (time until normalization of the SpO2 value) depending on the response time of the medical staff; c) Frequency of hypoxemic episodes over the course of the day depending on the type of touch (skin-to-skin care, physiotherapy, hands-on medical treatment, etc.)
- Secondary Outcome Measures
Name Time Method