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Postoperative Changes in Optic Nerve Sheath Diameter in Patients Undergoing Spinal Anesthesia for Cesarean Delivery | Clinical Trials | Clareo Health

UNKNOWN

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

NCT04301830•SMG-SNU Boramae Medical Center

View on ClinicalTrials.gov

Summary

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

Eligibility

Age

20 - No limit years

Sex

FEMALE

Healthy Volunteers

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.

Key Dates

Start Date

April 1, 2020

Primary Completion Date

April 1, 2021

Completion Date

April 1, 2022

Last Updated

March 10, 2020

Enrollment

ESTIMATED participants

Conditions

Intracranial Hypotension

Stent Implantation Versus Medical Therapy for Idiopathic IntracraniaL Hypertension (SIMPLE)

NCT05707442

Idiopathic Intracranial HypotensionVenous Sinus Stenosis

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ENROLLING_BY_INVITATION

Pathophysiology and Treatment of Cerebrospinal Hypotension Exploration Study

NCT06805591

Spontaneous Intracranial HypotensionIntracranial Hypotension+1 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 10, 2020Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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

Inclusion Criteria

Exclusion Criteria

Stent Implantation Versus Medical Therapy for Idiopathic IntracraniaL Hypertension (SIMPLE)

Pathophysiology and Treatment of Cerebrospinal Hypotension Exploration Study

Blind Versus Targeted Epidural Patch With Autologous Platelet-rich Plasma for Spontaneous Intracranial Hypotension

Spontaneous Intracranial Hypotension Treatment "SIHT"