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Optic Nerve Sheath Diameter in Preeclampsia

K

Kanuni Sultan Suleyman Training and Research Hospital

Status

Completed

Conditions

Pre-Eclampsia

Treatments

Diagnostic Test: Optic nerve sheath diameter measurement

Study type

Interventional

Funder types

Other

Identifiers

NCT04004897
Huseyin3

Details and patient eligibility

About

Severe preeclampsia is associated with an elevation in intracranial pressure (ICP). Optic nerve sheath diameter is a non-invasive surrogate of invasive ICP measurement. This study targets to evaluate the ICP in patients with or without preeclampsia.

Full description

MRI studies have shown that brain edema due to an elevation in ICP develops in up to 70% of women with preeclampsia. Optic nerve sheath diameter is used to estimate the ICP and has been shown to correlate well with invasive ICP measurement. The present study aims to compare ICP using optic nerve sheath diameter in women with or without preeclampsia.

Enrollment

90 patients

Sex

Female

Ages

18 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Must be diagnosed as preeclampsia
  • Age must be > 18 years

Exclusion criteria

  • History of previous intracranial pathology or surgery
  • Glaucoma

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

90 participants in 2 patient groups

Preeclampsia group
Other group
Description:
Patients with preeclampsia will receive optic nerve sheath diameter measurement with a linear ultrasound probe carefully and gently placed on the closed upper eyelids of patients.
Treatment:
Diagnostic Test: Optic nerve sheath diameter measurement
Pregnants without preeclampsia
Other group
Description:
Pregnant women without preeclampsia will receive optic nerve sheath diameter measurement with a linear ultrasound probe carefully and gently placed on the closed upper eyelids of patients.
Treatment:
Diagnostic Test: Optic nerve sheath diameter measurement

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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