Optic Nerve Sheath Diameter for Predicting Post-Dural Puncture Headache in Cesarean Section Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorKocaeli University

About this trial

Some patients develop headache after spinal anesthesia used during cesarean section. This condition is called post-dural puncture headache (PDPH). Early identification of patients at risk may improve patient care.

This study evaluates whether optic nerve sheath diameter (ONSD), measured using a non-invasive bedside ocular ultrasound technique, can help predict the development of PDPH.

Participants undergoing cesarean section with spinal anesthesia will undergo ONSD measurements at predefined perioperative time points. Participants will be followed postoperatively for the occurrence of headache.

The findings may help improve early recognition and management of PDPH.

Eligibility criteria

Qualifiers

Women aged 18 to 45 years

Singleton pregnancy

Planned cesarean section (elective or emergency due to fetal indications)

Spinal anesthesia planned for the procedure

Disqualifiers

Known ophthalmologic diseases affecting the optic nerve or retina (e.g., glaucoma, optic atrophy)

Active eye infection or recent ocular surgery

Known intracranial pathology affecting cerebrospinal fluid dynamics (e.g., intracranial mass, hydrocephalus, idiopathic intracranial hypertension)

History of stroke or subarachnoid hemorrhage

Trial design

Treatments tested in this trial

  • Optic Nerve Sheath Diameter Measurement

Treatment groups

No treatment groups listed

Sponsors and collaborators