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.
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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

Agathi Karakosta

+306948066243

akarakosta@uoi.gr

CONTACT

Dimitra Oikonomou

+306959136713

dimitra.oiknm@gmail.com

CONTACT