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New study aims to speed up pain relief during C-Sections

NCT ID NCT07349082

Symptom relief Sponsor: Gadjah Mada University 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compares two types of anesthesia for cesarean deliveries: standard epidural and a newer technique called dural puncture epidural (DPE). The goal is to see which one provides faster pain relief and better stability in blood pressure. Seventy-two pregnant women scheduled for C-sections will be randomly assigned to one of the two methods, and their pain block onset and side effects will be tracked.

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 DPE works faster, it could mean quicker pain relief and more stable blood pressure during C-sections.
What could go wrong
This is a small, early-stage trial with only 72 participants, so results may not apply to all patients. Both techniques have known risks like headache or low blood pressure.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 72 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

May 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.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

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 scheduled to undergo cesarean delivery * American Society of Anesthesiologists (ASA) physical status II-III * Willing to participate in the study by providing written informed consent Exclusion Criteria: * Patients with absolute contraindications to neuraxial anesthesia * Patients with known allergy or history of allergy to medications used in the study * Patients with psychiatric disorders or who are uncooperative * Patients with accidental dural puncture Dropout Criteria: * Patients who require conversion to general anesthesia during the procedure * Patients who experience major intraoperative complications (massive hemorrhage, shock, or cardiac arrest)

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As listed by the trial registrant

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

Cesarean section

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. 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

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Dr. Sardjito General Hospital

    Sleman, DI Yogyakarta, Indonesia

  • Persahabatan General Hospital

    Jakarta, DKI Jakarta, Indonesia

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