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Active, not recruiting Observational

The Effect of Magnesium on Post-spinal Headaches

NCT07502482 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-04-01
Last updated
2026-07-07

Condition(s) studied

Post-spinal Headache

Investigational drug(s) / intervention(s)

Magnesium

Magnesium: Post-spinal headache in patients receiving magnesium

Study summary

This retrospective cohort study aims to assess the effect of the use of magnesium sulphate in routine clinical practice on the development of post-dural puncture headache in patients undergoing spinal anaesthesia

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * • Patients aged 18-45 * Patients who underwent spinal anaesthesia for elective caesarean section * Patients with an ASA physical status score of I-III * Patients in whom a 25G or 27G pencil-point needle was used for spinal anaesthesia * Patients with complete medical records Exclusion Criteria: * • Patients undergoing emergency surgery * Patients with a history of chronic headaches * Patients who have undergone unsuccessful spinal anaesthesia or multiple attempts * Patients who have undergone combined spinal-epidural anaesthesia * Patients with a contraindication to magnesium sulphate * Patients with insufficient medical records

Primary outcome measure(s)

  • Incidence of post-spinal headache — 1. day
    the number of people who develop a headache following spinal anaesthesia

Trial sites (1)

FacilityCityRegionStatus
Haseki Training and Research Hospital Istanbul Sultangazi
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 NCT07502482 on ClinicalTrials.gov ↗ ← All trials in Turkey