Actively Recruiting

Phase 4
Age: 18Years +
FEMALE
NCT06797973

Efficacy and Safety of Intrathecal Morphine for Postoperative Pain Management Following Planned Caesarean Section

Led by Anne Juul Wikkelsø · Updated on 2025-12-19

1312

Participants Needed

8

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if morphine added to the spinal anaesthesia can improve postoperative pain treatment for patients undergoing caesarean section, without increasing the risk of serious adverse events in mother and baby. The main questions it aims to answer are: * Is the treatment effective in preventing postoperative pain? * Is the treatment safe for both mother and baby? Participants will be given a normal spinal anaesthesia with addition of either morphine or sodium chloride (inactive substance). All participants will receive standard postoperative pain treatment, including morphine tablets as needed. Researchers will collect data from the electronic medical record and ask the participants to fill out questionnaires about pain levels and possible side effects.

CONDITIONS

Official Title

Efficacy and Safety of Intrathecal Morphine for Postoperative Pain Management Following Planned Caesarean Section

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years or older
  • Singleton pregnancy
  • Scheduled for planned caesarean section under spinal anaesthesia
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Allergy or contraindication to trial medications
  • Planned postoperative epidural due to expected difficult pain management
  • Planned combined spinal-epidural as primary anaesthesia
  • Inability to understand and read Danish
  • Previous participation in this trial

AI-Screening

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Trial Site Locations

Total: 8 locations

1

Aarhus University Hospital

Aarhus, Denmark, 8200

Actively Recruiting

2

Copenhagen University Hospital - Rigshospitalet

Copenhagen, Denmark, 2100

Not Yet Recruiting

3

Copenhagen University Hospital - Herlev and Gentofte, Herlev

Herlev, Denmark, 2730

Not Yet Recruiting

4

Copenhagen University Hospital - North Zealand, Hillerød

Hillerød, Denmark, 3400

Not Yet Recruiting

5

Copenhagen University Hospital - Amager and Hvidovre, Hvidovre

Hvidovre, Denmark, 2650

Actively Recruiting

6

University Hospital of Southern Denmark - Lillebælt Hospital, Kolding

Kolding, Denmark, 6000

Actively Recruiting

7

University Hospital of Southern Denmark - Odense University Hospital

Odense C, Denmark, 5000

Actively Recruiting

8

Zealand University Hospital

Roskilde, Denmark, 4000

Actively Recruiting

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Research Team

A

Anneline B Seegert, MD

CONTACT

A

Anne J Wikkelsø, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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