Actively Recruiting
Frequency of Occurrence and Risk Factors of Postoperative Nausea and Vomiting During Elective C-section Under Spinal Anesthesia With Preventive Medication
Led by University of Liege · Updated on 2025-04-15
400
Participants Needed
2
Research Sites
54 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to learn about the incidence and risk factors of nausea and vomiting during planned caesarean section under spinal anesthesia. The main question it aims to answer is : What are the incidence and risks factors of postoperative nausea and vomiting (NV) during planned caesarean section under spinal anesthesia with administration of intrathecal morphine and multimodal antiemetic prophylaxis ? Patients who will be managed according to the standard protocol in use in the department will have to answer specific questions about NV in the post-interventional recovery room and on 2 further visits in the first 24 hours post-caesarean section.
CONDITIONS
Official Title
Frequency of Occurrence and Risk Factors of Postoperative Nausea and Vomiting During Elective C-section Under Spinal Anesthesia With Preventive Medication
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients requiring elective cesarean section under spinal anesthesia
- Pregnancy with a single fetus
- Gestational age greater than 37 weeks of amenorrhea
You will not qualify if you...
- Unable to understand French
- Contraindication to locoregional anesthesia
- Nausea or vomiting within 24 hours before the procedure
- Insulin-requiring type 1 or type 2 diabetes not related to pregnancy
- Allergy or contraindication to medications used in the standard management protocol
- Severe preeclampsia
- Height less than 150 cm
AI-Screening
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Trial Site Locations
Total: 2 locations
1
CHU de Liège - site de Notre-Dame des Bruyères
Chenée, Belgium, 4032
Actively Recruiting
2
Hôpital de la Citadelle - site Citadelle
Liège, Belgium, 4000
Not Yet Recruiting
Research Team
T
Thibault Michot, M.D.
CONTACT
F
Fernande J Lois, M.D., PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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