Chinese University of Hong Kong
Hong Kong, China
NCT Number: NCT03002051
To evaluate clinical efficacy and safety of a novel lumen-apposing FCSEMS for EUS-guided transenteric drainage of PFC or of biliary tree including GB
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Notify Me20 year–80 year
All sexes
Interventional
Not applicable
Hong Kong, China
Patients with the following conditions would be recruited for drainage under EUS guidance with the new lumen apposing FCSEMS
Outcome paramaters include technical and clinical success, adverse events.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patient must meet all of the following inclusion criteria to be eligible for enrollment into the study.
Exclusion criteria
Patient presenting with any of the following will not be included in the study.
Time frame: 8 hrs
① Clinical success of pancreatic fluid collections
Time frame: 8hrs
Time frame: 2 weeks
Time frame: 1 day
Time frame: 30 day
Chinese University of Hong Kong
Other
EUS-guided Transenteric Drainage With a Novel Lumen-apposing Metal Stent for the Management of Pancreato-biliary Diseases: a Multi-national, Multicenter Prospective Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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