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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02761954
Other study ID # Kaudal Studie
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date December 20, 2017

Study information

Verified date July 2018
Source Bürgerhospital Frankfurt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

With this study we want to see how the blood flow in the anterior cerebral artery (ACA) and the basilar artery (BA) after the caudal block changes.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 20, 2017
Est. primary completion date December 20, 2017
Accepts healthy volunteers No
Gender All
Age group N/A to 12 Months
Eligibility Inclusion Criteria:

- opened big fontanella

- infraumbilical surgery

Exclusion Criteria:

- cardiac or cerebral disease

- prior operation on vertebra, heart or head/brain

- malforamtion of head or vertebra

- closed fontanella

- contraindication for caudal block (von-Willebrand-Syndrome, haemophilia,...)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bürgerhospital Frankfurt

Outcome

Type Measure Description Time frame Safety issue
Primary depression of blood flow in ACA & basilar artery after caudal block one hour
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