Determining the Optimal Dose of Intrathecal Morphine for Post-Cesarean Analgesia
Recruiting
N/A
Interventional Study
Morphine
Cesarean Section
Postoperative Pain, Acute
Spinal Analgesia
Postoperative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- University of Ioannina · Other
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About This Trial
Using spinal or epidural anesthesia (known as neuraxial blocks) is the gold standard for pain control during childbirth, especially in cesarean sections (C-sections). However, many women experience moderate to severe pain after a C-section, which can affect both their physical and emotional well-being, and even impact their ability to care for their newborn. Unfortunately, this pain is often not t…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* term parturient
* single pregnancy
* elective cesarean delivery
* adult parturient
* ASA II
Exclusion Criteria:
* participants under the age of 18
* extreme somatometric characteristics
* lack of patient consent
* absolute contraindications for spinal anesthesia
* urgent ces…
Contacts