Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

New C-Section pain protocol shows promise in reducing severe pain

NCT ID NCT06813638

Symptom relief Sponsor: Nordsjaellands 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether adding a numbing injection into the wound and a steroid medication during a planned C-section could lower the number of women experiencing severe pain after surgery. The researchers compared pain scores before and after making this change in 100 women. The goal was to see if these simple steps could make recovery more comfortable.

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

100 people

The number who actually took part.

Started

Jan 2025

Finished

Jun 2025

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

Elective CS Patients at our center will be approached for inclusion in the postoperative care unit shortly after the CS during the study period

Ages

18 years and older

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 who undergo planned cesarean section under spinal anesthesia. * Patients who speak and read Danish and can provide informed consent to participate. * Patients who have a mobile phone that can receive a text message with a link to a questionnaire that can be accessed on an online website on the phone. * Age ≥ 18 years Exclusion criteria: * The study excludes patients with daily opioid use. * Multiple pregnancies (gemelli or more). * Insulin-treated diabetes. * Chronic pain patients. * Unplanned CS

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Cesarean delivery are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

agnosia Pain, Postoperative

As listed by the trial registrant

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

Cesarean delivery Cesarean section Cohort study Pain management Pain management in postoperative care Patient reported outcome Postoperative pain Text message Wound infiltration

Contacts and locations

Locations

  • University Hospital of Copenhagen, Northern Zealand

    Hillerød, 3400, Denmark

More trials for these conditions

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