Actively Recruiting
Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery
Led by Ente Ospedaliero Cantonale, Bellinzona · Updated on 2026-03-16
63
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Based on randomization, patients will receive a mixture for spinal anesthesia and will be followed in the following hours for the various outcomes and for functional recovery
CONDITIONS
Official Title
Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years of age
- Height over 160 cm
- American Society Anesthesiologists physical status I or II
- Term singleton pregnancies
- Scheduled for elective cesarean delivery under spinal anesthesia at Ospedale Regionale Bellinzona Valli
You will not qualify if you...
- Inability to give consent
- Patient refusal
- Contraindications to spinal anesthesia such as hemodynamic instability, infection at surgery site, or neurologic defects like transverse myelitis
- Emergency cesarean delivery
- Preeclampsia or eclampsia
- Allergy to any drugs used in the study protocol
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ospedale Regionale di Bellinzona, San Giovanni
Bellinzona, Switzerland
Actively Recruiting
Research Team
R
Roberto Dossi
CONTACT
A
Alessandra Lauretta
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here