Evaluation of the Value of Ultrasound Measurement of Stomach Diameter in Predicting Postoperative Nausea/Vomiting

Recruiting N/A Interventional Study
Patient With Indication for Major Abdominal Submesocolic, Parietal, Left Pancreatic or Liver Surger
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
150 (estimated)
Sponsor
University Hospital, Angers · Government
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About This Trial
The advent of enhanced rehabilitation after surgery has helped to reduce surgical stress, thereby improving postoperative outcomes by reducing the time it takes for patients to recover their transit and autonomy. Despite this, some 10-30% of patients undergoing abdominal surgery will experience postoperative ileus or nausea/vomiting. In addition to increasing the length of hospital stay, these co…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Major patient * Indication for major abdominal surgery (submesocolic, parietal, left pancreas or liver) * Patient affiliated to or benefiting from a social security scheme Non-inclusion criteria * Patient refusal to participate in study * Need for immediate post-operative IC…
Contacts

Jean-Baptiste Philippe, MD

0241353618

JeanBaptiste.Philippe@chu-angers.fr

CONTACT

Aurelien Venara, MD, PhD

0241353618

auvenara@chu-angers.fr

CONTACT