Comparison of Optic Nerve Sheath Diameter on Retrobulbar Ultrasound Before and After Drainage of Cerebrospinal Fluid in Patient With Hydrocephalus

Sponsor
Yonsei University (Other)
Overall Status
Terminated
CT.gov ID
NCT01863329
Collaborator
(none)
15
1
6
2.5

Study Details

Study Description

Brief Summary

Studies in patients with intracranial hypertension have shown a good relationship between optic nerve sheath diameter measured by retrobulbar ultrasound and invasively measured intracranial pressure. The aim of this study was to evaluate changes in optic nerve sheath diameter before and after drainage of cerebrospinal fluid in patients with hydrocephalus.

Condition or Disease Intervention/Treatment Phase
  • Procedure: retrobulbar ultrasound

Study Design

Study Type:
Observational
Actual Enrollment :
15 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Sep 1, 2013

Arms and Interventions

Arm Intervention/Treatment
both optic nerve sheath diameter

both optic nerve sheath diameter (the posterior 3mm of the papilla), 5 individual measurement

Procedure: retrobulbar ultrasound
both optic nerve sheath diameter (the posterior 3mm of the papilla), 5 individual measurement

Outcome Measures

Primary Outcome Measures

  1. both optic nerve sheath diameter (the posterior 3mm of the papilla) [from induction of general anesthesia to average 15 min after recovery of general anesthesia]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. ASA Ⅰ-Ⅱ

  2. aged between 20 and 70 year

  3. hydrocephalus

  4. general anesthesia for undergoing drainage of cerebrospinal fluid

Exclusion Criteria:
  1. an anatomical or functional abnormality in optic nerve

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine Seoul Korea, Republic of 120-752

Sponsors and Collaborators

  • Yonsei University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yonsei University
ClinicalTrials.gov Identifier:
NCT01863329
Other Study ID Numbers:
  • 4-2013-0006
First Posted:
May 27, 2013
Last Update Posted:
Mar 27, 2019
Last Verified:
Dec 1, 2014
Keywords provided by Yonsei University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2019