„Hemodynamic implications of epidural anaesthesia in Neonates, Infants and Children”

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00004201

Enrollment

Registered

2014-06-04

Start date

2014-01-14

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

epidural anesthesia for thoracal or abdominal surgery

Interventions

Group 1: we will record hemodynamic changes after epidural anesthesia in 50 children via LIDCO /INVOS monitoring

Eligibility

Sex/Gender

All

Age

0 Years to 6 Years

Inclusion criteria

Inclusion criteria: Neonates, infants and children under the age of six years scheduled for major abdominal surgery will be included in the study

Exclusion criteria

Exclusion criteria: Patients who are already included into another clinical trial - Parents and or patients refusal to participate the study - Any contraindication for epidural anaesthesia like neurological disorders, coagulation disorders thrombocytopenia, severe sepsis, known allergic reaction to local anaesthetic, local infection on the injection site or spine malformations

Design outcomes

Primary

Measure	Time frame
What: Record hemodynamic changes after epidural anesthesia. When: we will measure from the beginning until the end of surgery with the LIDCO /INVOS monitoring	—

Secondary

Measure	Time frame
there is no secondary endpoint	—

Countries

Austria

Contacts

Public ContactLydia Triffterer

AKH Wien

lydia.triffterer@meduniwien.ac.at0043 1 19231

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026