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Study identifier: NCT06927830 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Frequency of Occurrence and Risk Factors of Postoperative Nausea and Vomiting During Elective C-section Under Spinal Anesthesia With Preventive Medication

Condition: Nausea and Vomiting, Postoperative · Cesarean Delivery · Spinal Anesthesia  ·  Sponsor: University of Liege

PhaseN/A
Planned participants400
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Thibault Michot, M.D.  ·  +32 4 3234141  ·  tmichot@chuliege.be

Fernande J Lois, M.D., PhD  ·  fernande.lois@chuliege.be

Always discuss trial participation with your own doctor first.

Locations (2)

CHU de Liège - site de Notre-Dame des BruyèresChenée, BelgiumRecruiting
Hôpital de la Citadelle - site CitadelleLiège, BelgiumNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06927830