Status:
RECRUITING
Frequency of Occurrence and Risk Factors of Postoperative Nausea and Vomiting During Elective C-section Under Spinal Anesthesia With Preventive Medication
Lead Sponsor:
University of Liege
Conditions:
Nausea and Vomiting, Postoperative
Cesarean Delivery
Eligibility:
FEMALE
18+ years
Brief Summary
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 a...
Eligibility Criteria
Inclusion
- Any patient requiring elective caesarean section under spinal anesthesia, at a gestational age \>37 weeks of amenorrhea in the context of a single-fetal pregnancy.
Exclusion
- Failure to understand the French language; Contraindication to locoregional anesthesia; Nausea and/or vomiting in the 24 hours preceding the procedure; Type 1 or type 2 insulin-requiring non-gestational diabetes; Allergy or contraindication to one of the products used in the usual management protocol; Severe preeclampsia; Height \<150 cm
Key Trial Info
Start Date :
March 19 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
April 1 2026
Estimated Enrollment :
400 Patients enrolled
Trial Details
Trial ID
NCT06927830
Start Date
March 19 2025
End Date
April 1 2026
Last Update
April 15 2025
Active Locations (2)
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1
CHU de Liège - site de Notre-Dame des Bruyères
Chenée, Belgium, 4032
2
Hôpital de la Citadelle - site Citadelle
Liège, Belgium, 4000