Phase
Condition
Constipation
Ileus
Treatment
inert tablet
Naloxegol
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
> 18 years old,
Undergoing cardiac surgery with cardiopulmonary bypass,
For women of child bearing potential without contraception, beta-HCG negative result
Having signed a written informed consent form,
Affiliation to the social security system.
Exclusion
Exclusion Criteria:
Allergy or known hypersensitivity to Naloxegol or any of the excipients or any otheropioid antagonist
Pregnant or breastfeeding women
Severe hepatic failure, history of cirrhosis
Moderate or severe renal failure (GFR<60ml/min)
Concomitant treatment with a strong cytochrome P450 3A4 inhibitor
History of acute gastro-intestinal obstruction known or suspected
History of digestive arteritis
Clinically relevant alteration of the blood-brain-barrier
Cancer with increased risk of gastro-duodenal perforation
Disorder that could alter the integrity of the gastrointestinal lining
Regular treatment with laxative drugs
Concomitant treatment with methadone
Patient unable to take a drug by oral route
Patient under protection of the adults (guardianship, curators or safeguard ofjustice),
Patient included or planning to be included in another research protocol relating tomedications.
Study Design
Study Description
Connect with a study center
CMC Ambroise Paré
Neuilly-sur-Seine, Neuilly Sur Seine 92200
FranceSite Not Available

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