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

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04301830

Enrollment

Registered

2020-03-10

Start date

2020-04-30

Completion date

2022-04-30

Last updated

2020-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracranial Hypotension

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to No maximum

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.

Design outcomes

Primary

Measure	Time frame	Description
Change optic nerve sheath diameter	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

Outcome results