Monitoring of systemic and regional perfusion in preterms, newborns and infants under awake caudal anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00015742

Enrollment

Registered

2018-10-30

Start date

2018-07-18

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

hypotension I95

Interventions

Group 1: The cardiac index and the cerebral oximetrie are measured non invasive, additionaly to the standard Monitoring, in preterms and newborns with operations under awake caudal anesthesia.

Eligibility

Sex/Gender

All

Age

No minimum to 2 Months

Inclusion criteria

Inclusion criteria: informed consent for surgery under awake caudal anesthesia

Exclusion criteria

Exclusion criteria: no informed consent

Design outcomes

Primary

Measure	Time frame
Evaluation of data of systemic and regional Perfusion under awake caudal anesthesia	—

Secondary

Measure	Time frame
Advantage of awake caudal anesthesia for the postoperativ progress (discharge time from recovery room, start of enteral feeding)	—

Countries

Germany

Contacts

Public ContactChristiane Beck

Medizinische Hochschule Hannover

beck.christiane@mh-hannover.de017615323661

Outcome results

None listed

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