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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03066024
Other study ID # Retro-Child
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2015
Est. completion date December 2015

Study information

Verified date April 2020
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

As part of the clinical routine of the Department of Anesthesiology and Intensive Care Medicine CVK/CCM in the Charité - University Medicine Berlin intraoperative electroencephalography data and clinical routine data are recorded and evaluated in surgical children and adolescents according to different age groups.


Recruitment information / eligibility

Status Completed
Enrollment 94
Est. completion date December 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Children and adolescents undergoing surgery procedure

Exclusion Criteria:

- Neurosurgery

- Pre-existing neurological conditions

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Department of Anesthesiology and Intensive Care Medicine CVK/CCM, Charité - University Medicine Belrin Berlin

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Electroencephalography monitoring changes Up to the end of surgery
Secondary Anesthetic depth Up to the end of surgery
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