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Clinical Trials in China / NCT06800859
Enrolling by invitation Observational

Establishment of a Predictive Model for Post-dural Puncture Headache

NCT06800859 · tracked via the Priya Life Science China tracker
Sponsor
Yilin Zhao
Phase
Observational
Started
2025-01-20
Last updated
2025-01-30

Condition(s) studied

Spinal and Epidural Anaesthesia-Induced Headache During Pregnancy

Investigational drug(s) / intervention(s)

Supplement fluids

Supplement fluids: To ensure optimal recovery and manage potential complications, patients are advised to supplement fluids by increasing their oral intake or receiving intravenous fluids as necessary. Bed rest is recommended to reduce physical strain and promote healing. Additionally, a blood patch procedure may be performed to alleviate symptoms such as headaches that can occur after certain medical procedures, particularly spinal taps. This involves injecting a small amount of the patient's own blood into the epidural space to seal any leaks of cerebrospinal fluid, thereby providing relief and aiding in recovery. Proper monitoring and follow-up care are essential to ensure the effectiveness of these interventions

Study summary

The goal of this clinical trial is to establish a predictive model for post-dural puncture headache. The main questions it aims to answer are:

Changes in intracranial pressure after spinal puncture (or lumbar puncture). When post-dural puncture headache occurs, the optic nerve sheath diameter (ONSD) change When the optic nerve sheath diameter (ONSD) and (or) Intraocular Pressure (IOP) reaches a certain threshold, does proactive treatment reduce the incidence of postoperative headaches? Researchers will measure the optic nerve sheath diameter (ONSD) using ultrasound and ( or ) magnetic resonance imaging (MRI) before and after spinal puncture.

Researchers will measure the Intraocular Pressure (IOP) using ICARE before and after spinal puncture.

Participants will:

Undergo ultrasound and (or) magnetic resonance imaging (MRI) examinations before and after spinal puncture Undergo ICARE examinations before and after spinal puncture

Eligibility

Sex
ALL
Min age
3 Years
Max age
34 Years
Healthy volunteers
No
Inclusion Criteria: BMI ≤ 30 kg/m² Normal liver and kidney function before surgery Normal coagulation function before surgery Hemoglobin \> 70 g/L Platelet count \> 80 × 10⁹/L Exclusion Criteria: Patients who experience major bleeding during or after surgery Patients with cerebrospinal fluid leakage or other serious malformations Patients with mental health disorders or cognitive dysfunction

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tongji Hospital of Tongji Medical College of Huazhong Universtiy of Science and Technology Wuhan Hubei

More Yilin Zhao trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06800859 on ClinicalTrials.gov ↗ ← All trials in China