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

This trial does not accept healthy volunteers

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 population

The study population will consist of pregnant women aged 18-45 years undergoing cesarean section under spinal anesthesia at Kocaeli University Hospital. Participants who meet the eligibility criteria and provide informed consent will be enrolled.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Optic Nerve Sheath Diameter Measurement

    Other intervention

    Participants will undergo non-invasive ocular ultrasound measurement of optic nerve sheath diameter at five predefined time points: preoperatively, 10 minutes after spinal anesthesia, at the end of surgery, at postoperative 24 hours, and at postoperative 48 hours.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Association Between Optic Nerve Sheath Diameter Measurements and Post-Dural Puncture Headache

Assessment of the association between optic nerve sheath diameter measurements and the development of post-dural puncture headache.

Time frame
Within 48 hours after spinal anesthesia

Secondary outcomes

Other outcomes

Sponsors and contacts

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