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Clinical Trials/NCT04301830
NCT04301830
Unknown
Not Applicable

Postoperative Changes in Optic Nerve Sheath Diameter in Patients Undergoing Spinal Anesthesia for Cesarean Delivery

SMG-SNU Boramae Medical Center0 sites50 target enrollmentApril 2020
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ConditionsIntracranial Hypotension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intracranial Hypotension
Sponsor
SMG-SNU Boramae Medical Center
Enrollment
50
Primary Endpoint
Change optic nerve sheath diameter
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

This is observational study. The investigator will measure optic nerve sheath diameter by ultrasound on the eye after cesarean section under spinal anesthesia.

Registry
clinicaltrials.gov
Start Date
April 2020
End Date
April 2022
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jin-Young Hwang

Associate professor

SMG-SNU Boramae Medical Center

Eligibility Criteria

Inclusion Criteria

  • •Patients undergoing cesarean section under spinal anesthesia

Exclusion Criteria

  • •Patients who did not agree to participate in the study
  • •Patients has ophthalmic diseases
  • •Patients has previous history of ophthalmic surgery.
  • •Patients has neurological disorders.
  • •Patients has history of head surgery.

Outcomes

Primary Outcomes

Change optic nerve sheath diameter

Time Frame: 0,1,6,24 and 48 hours

Change in Optic nerve sheathe diameter from baseline, 1,,6,24 and 48 hours after completion of surgery

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