Intrathecal Versus Epidural Morphine for Post-Cesarean Analgesia
Recruiting
Phase 4
Interventional Study
Analgesia Obstetrical
Analgesia
Post Operative Pain
Patient Satisfaction
Cesarean Section Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 120 (estimated)
- Sponsor
- Hospital Central do Funchal · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
Cesarean section is one of the most commonly performed surgical procedures worldwide, making effective management of acute postoperative pain a key issue in obstetric anesthesiology. Post-cesarean analgesia should promote rapid maternal recovery, support newborn care, and consider the pharmacological implications for breastfeeding.
According to recent PROSPECT® guidelines from ESRA, neuraxial opi…
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria:
* Pregnant women scheduled for elective cesarean section;
* Age \> 18 years;
* Willingness to participate in the study, as demonstrated by signed informed consent.
Exclusion Criteria:
* American Society of Anesthesiologists (ASA) physical status classification \> III;
* Chroni…
Contacts
No contact information available.