Clinical Trials in Turkey / NCT07502482
Active, not recruiting
Observational
The Effect of Magnesium on Post-spinal Headaches
NCT07502482 · tracked via the Priya Life Science Turkey tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Haseki Training and Research Hospital | Istanbul | Sultangazi |
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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