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Spinal headache study: does pregnancy affect pain after anesthesia?

NCT ID NCT06992063

What the study statuses mean

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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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 112 women who had spinal anesthesia for surgery to see how often they got post-dural puncture headaches and how severe they were. Researchers compared pregnant women (obstetric) to non-pregnant women (non-obstetric) to find out if pregnancy changes headache risk. Participants reported their pain using simple scales, and anxiety levels were also measured before surgery.

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

112 people

The number who actually took part.

Started

May 2025

Finished

Jan 2026

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

Obstetric and non-obstetric female patients undergoing spinal anesthesia

Ages

18 to 65 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Female patients aged 18-65 years undergoing surgery under spinal anesthesia * Patients classified as ASA I or II according to the American Society of Anesthesiologists (ASA) classification Exclusion Criteria: * ASA III and above patients * Patients requiring Intensive Care Unit (ICU) admission * Patients with mental retardation * Patients with communication difficulties (e.g., hearing loss, speech impediments, language barriers) * Conversion to general anesthesia due to pain after spinal anesthesia * Emergency surgeries

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Conditions

The condition(s) this trial relates to.

intracranial hypotension Post-Dural Puncture Headache

As listed by the trial registrant

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

Contacts and locations

Locations

  • Duzce University Faculty of Medicine

    Düzce, Düzce, 81000, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.