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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04412109
Other study ID # 2020-01-081
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 25, 2020
Est. completion date November 16, 2020

Study information

Verified date November 2020
Source Keimyung University Dongsan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Valid method of indirect measurement of intracranial pressure is using optic nerve sheath diameter. Different volume of injection is known to affect the degree of increase of intracranial pressure. This study is desinged to measure the changes of optic nerve sheath diameter and cerebral oxygenation when different volume of normal saline was injected.


Description:

Previous study showed that different volume of injections (1.0 ml/kg vs. 1.5 ml/kg) during caudal anesthesia showed siginifiant increase of optic nerve sheath diameter in group of high volumes. Increase of ICP can result in harmful effect including reduced cerebral flow and oxygen saturation. Also, increase of ICP can cause headache, syncope and transient loss of visual acuity. The proven and valid method of measuring ICP indirectly is using optic nerve sheath diameter. This study was designed to examine the changes of optic nerve sheath diameter and cerebral oxygenation when different volume of normal saline was injected.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 16, 2020
Est. primary completion date November 16, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - lung cancer - liver cancer - stomach cancer - pancreas cancer - gallbladder cancer Exclusion Criteria: - coagulopathy - infection - previous spine fusion at thoracic level - previous brain lesion causing increased intracranial pressure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
thoracic epidural catheterization
thoracic epidural catheterization for postoperative pain control

Locations

Country Name City State
Korea, Republic of Hong ji HEE Daegu

Sponsors (1)

Lead Sponsor Collaborator
Keimyung University Dongsan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary optic nerve sheath change during 4 time period optic nerve sheath change during 4 time period using ultrasound Baseline, 10 minutes, 20 minutes, 40 minutes after the completion of the intervention
Secondary cerebral oxygenation change during 4 time period cerebral oxygenation change during 4 time period using pressure monitoring kit Baseline, 10 minutes, 20 minutes, 40 minutes after the completion of the intervention
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