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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04134221
Other study ID # 1910-055-106
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 18, 2019
Est. completion date February 17, 2021

Study information

Verified date April 2021
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Little is known about how general anesthesia-induced decrease in cerebral blood flow in pediatric moyamoya pateints. We investigated this question in patients undergoing moyamoya surgery, hypothesizing that cardiorespiratory changes during this procedure would reduce cerebral perfusion.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 17, 2021
Est. primary completion date February 17, 2021
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - pediatric patients undergoing encephaloduroarteriosynangiosis surgery for moyamoya disease Exclusion Criteria: - cutaneous lesion on the neck

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Ultrasound assessment
Ultrasound assessment of internal carotid artery blood flow

Locations

Country Name City State
Korea, Republic of Hee-Soo Kim Seoul Soul-t'ukpyolsi

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Internal carotid artery blood flow velocity ultrasound assessment of internal carotid artery blood flow velocity from anesthetic induction to end of surgery, an average of 5 hours