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Blood test markers may forecast spinal headache risk in cesarean patients

NCT ID NCT07706751

Knowledge-focused Sponsor: Amasya University Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time

Summary

This study looks at whether simple inflammation markers from routine blood tests can predict postdural puncture headache (PPH) in pregnant women having a cesarean section under spinal anesthesia. Researchers will analyze pre- and post-surgery blood results from 260 women to see if certain inflammation values are linked to developing PPH. The goal is to identify at-risk women early so preventive steps can be taken.

What this could mean

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

What this could lead to
If successful, this could help doctors identify women at risk for postdural puncture headache early and take steps to prevent it.
What could go wrong
This is an observational study, so it cannot prove cause and effect. The results may not apply to all patients or settings.

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

About 260 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 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

Pregnant women undergoing cesarean section under spinal anesthesia

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: * . Pregnant women who are of a cognitive level capable of giving informed consent * Pregnant women aged 18-45 who have undergone elective cesarean section * Term (37 weeks and above) pregnant women * Patients with an American Society of Anesthesiologists (ASA) physical status score of 2 (ASA II) Exclusion Criteria: * History of active infection or chronic inflammatory disease * History of steroid or immunomodulatory drug use * Presence of coagulopathy or hematological disorder * Presence of preeclampsia/HELLP syndrome * Those who received blood transfusions during and after surgery

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As listed by the trial registrant

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

Headache after spinal puncture Pregnancy

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Amasya University Training and Research Hospital

    RECRUITING

    Amasya, 05100, Turkey (Türkiye)

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