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Magnesium may stop Post-Spinal headaches in new moms

NCT ID NCT07502482

Symptom relief Sponsor: Haseki Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jul 08, 2026 · Updated 3 times

Summary

This study will review the medical records of 300 women who had a planned C-section under spinal anesthesia. Researchers want to see if those who received magnesium had fewer headaches afterward. The goal is to find a simple way to prevent this common side effect.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
magnesium sulphate
What this could lead to
If it works, this could point toward a simple way to reduce headaches after spinal anesthesia for C-sections.
What could go wrong
This is a small, early-stage study that only looks back at past records, so it can't prove cause and effect. The results may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

300 people

The number who actually took part.

Started

Apr 2026

Expected to finish

Sep 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

In this study, which is designed as a retrospective cohort study, the records of all patients who underwent caesarean section under spinal anaesthesia at our hospital between 1 January 2025 and 31 December 2025 and who met the inclusion criteria will be reviewed.

Ages

18 to 45 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Post-Dural Puncture Headache intracranial hypotension prevention target

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Post-spinal headache

Contacts and locations

Locations

  • Haseki Training and Research Hospital

    Istanbul, Sultangazi, Turkey (Türkiye)