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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03200951
Other study ID # 4-2017-0341
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 22, 2017
Est. completion date May 31, 2018

Study information

Verified date October 2018
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ultrasonography of optic nerve sheath diameter shows a good level of diagnostic accuracy for detecting intracranial hypertension. The aim of this study is to evaluate the effect of epidural block on intracranial pressure in pediatric patients with cerebral palsy undergoing osteotomy of lower extremity. Forty patients, aged 4 years to 13 years, receiving epidural block before osteotomy will be divided into bolus group (n=20) and infusion group (n=20). Randomly selected patients of the bolus group are given 0.3 ml/kg bolus of 0.15% ripivacaine for epidural block. In contrast, patients in the infusion group are given 0.3 ml/kg/hr 0.15% ripivacaine for epidural block. The primary endpoint is the difference in the optic nerve sheath diameter after epidural block measured by optic nerve ultrasonography between groups.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date May 31, 2018
Est. primary completion date May 31, 2018
Accepts healthy volunteers No
Gender All
Age group 4 Years to 13 Years
Eligibility Inclusion Criteria:

- Pediatric patients with cerebral palsy from 4 to 13 years of age undergoing osteotomy

- Body weight = 40 kg

Exclusion Criteria:

- Patients with contraindications to epidural analgesia (local infection, clotting disorders, anatomical abnormalities, sepsis, etc.)

- Patients with symptoms or signs associated with a history of elevated intracranial pressure or elevated intracranial pressure

- Patients with ophthalmic disease or surgery

- The estimated operation time is less than 70 minutes.

- All parents of the subject are foreigners or illiterate

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bolus group for epidural block
Randomly selected patients of the bolus group are given 0.3 ml/kg bolus of 0.15% ripivacaine for epidural block.
Infusion group for epidural block
Randomly selected patients of the infusion group are given 0.3 ml/kg/hr 0.15% ripivacaine for epidural block.

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institue, Yonsei Universiy College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (2)

Lin Y, Li Q, Liu J, Yang R, Liu J. Comparison of continuous epidural infusion and programmed intermittent epidural bolus in labor analgesia. Ther Clin Risk Manag. 2016 Jul 14;12:1107-12. doi: 10.2147/TCRM.S106021. eCollection 2016. — View Citation

Padayachy LC, Padayachy V, Galal U, Pollock T, Fieggen AG. The relationship between transorbital ultrasound measurement of the optic nerve sheath diameter (ONSD) and invasively measured ICP in children. : Part II: age-related ONSD cut-off values and patency of the anterior fontanelle. Childs Nerv Syst. 2016 Oct;32(10):1779-85. doi: 10.1007/s00381-016-3068-4. Epub 2016 Sep 20. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The difference in the optic nerve sheath diameter(ONSD) between groups The optic nerve sheath diameter measured by optic nerve ultrasonography. 5 minutes before epidural block
Primary The difference in the optic nerve sheath diameter(ONSD) between groups The optic nerve sheath diameter measured by optic nerve ultrasonography. 1 second after epidural block
Primary The difference in the optic nerve sheath diameter(ONSD) between groups The optic nerve sheath diameter measured by optic nerve ultrasonography. 10 minutes after epidural block
Primary The difference in the optic nerve sheath diameter(ONSD) between groups The optic nerve sheath diameter measured by optic nerve ultrasonography. 70 minutes after epidural block
Secondary The difference in the number of patients whose ONSD values increased to more than 5.75 mm at each time point between the two groups The optic nerve sheath diameter measured by optic nerve ultrasonography 5 minutes before epidural block
Secondary The difference in the number of patients whose ONSD values increased to more than 5.75 mm at each time point between the two groups The optic nerve sheath diameter measured by optic nerve ultrasonography 1 second after epidural block
Secondary The difference in the number of patients whose ONSD values increased to more than 5.75 mm at each time point between the two groups The optic nerve sheath diameter measured by optic nerve ultrasonography 10 minutes after epidural block
Secondary The difference in the number of patients whose ONSD values increased to more than 5.75 mm at each time point between the two groups The optic nerve sheath diameter measured by optic nerve ultrasonography 70 minutes after epidural block
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