Clinique Paris-Bercy
Charenton-le-Pont, 94220, France
NCT Number: NCT06535490
Large prospective comparative observational study in numerous reference centers in France, comparing infectious complications in patients admitted for pancreatic cystic lesions (PCL) aspiration performed with or without antibiotic prophylaxis (ATBp) according to the usual practices.
This is a prospective, comparative, observational, multicenter study, with the primary objective of comparing the infection rates in pancreatic cystic lesions (PCL) aspirated under EUS, with and without the administration of ATBp.
A sample size of 1702 patients will be needed over a 3-year study period.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Charenton-le-Pont, 94220, France
The complication rate after EUS fine needle aspiration (EUS-FNA) for pancreatic cystic lesions (PCL) is low, around 1-3% according to various series. However, it has long been recommended to perform this procedure under antibiotic prophylaxis (ATBp). Due to the risk of developing resistance to certain classes of antibiotics and the risk of complications, particularly allergic reactions, the role of ATBp in this indication needs to be reconsidered. The latest recommendations from European and French societies do not support the systematic formal indication of ATBp for aspiration under EUS. Because the literature on the subject is sparse and equivocal, practices remain varied (some performing PCL aspirations with and others without ATBp), and scientific societies do not provide a formal stance on the benefit of such ATBp. Therefore, we decided to conduct a very large prospective comparative observational study in numerous reference centers in France (centers of the Research and Action Group in Endoscopy - GRAPHE), comparing infectious complications in patients admitted for EUS-FNA for PCL performed with or without ATBp according to the usual practices .
This is a prospective, comparative, observational, multicenter study.
Primary objective:
Comparison of infection rates after EUS-FNA for pancreatic cystic lesions (PCL) , with and without the administration of ATBp.
Secondary objectives:
Rates of other infectious complications (pulmonary, urinary, etc.) Rates of post-ATBp complications, particularly allergic reactions Prolongation of scheduled hospitalization Evaluation of factors associated with post-EUS aspiration infection of PCL
After the endoscopic exploration, the patient will be monitored for the potential occurrence of complications related to EUS (perforation, hemorrhage, infection, allergy, etc.). Any adverse events will be recorded at 30 days post-procedure.
A sample size of 1702 patients will be needed over a 3-year study period.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Puncture of pancreatic cystic lesion with a fine needle under EUS guidance
Other names: EUS fine needle aspiration
Antibiotic prophylaxis consists of a single intravenous administration before or at the beginning of the procedure according to the common practices of each practitioner or unit
Other names: Antibiotic prophylaxis
Time frame: 30 days
Post-EUS-FNA infection rate of PCL (patients exhibiting clinical and biological signs - fever >38.5°C, neutrophilic leukocytosis, elevated CRP, pathogen identification in blood cultures - indicative of sepsis requiring prolonged antibiotic therapy). The occurrence of the aforementioned clinical and biological signs, along with imaging evidence (such as cyst wall thickening or presence of intracystic air images) and the absence of another infection source (urinary, pulmonary, venous, etc.) will lead to the diagnosis of post-FNA infection. Centralized validation of infection cases will be conducted by an expert panel based on clinical, biological, and imaging findings.
Time frame: 30 days
Number of patients with at least one urinary infection within 21-30 days after EUS-FNA
Time frame: 30 days
Number of patients with at least one allergic reaction within 21-30 days after EUS-FNA
Time frame: 30 days
Number of hospitalization days per stay within 30 days following EUS-FNA
Time frame: 1 days
25G, 22G, 20G, or 19G
Time frame: 1 days
Yes or No
Time frame: 1 day
Thin, thick, hemorrhagic
Time frame: 1 day
Yes or No
Time frame: 30 days
mucinous vs. non-mucinous
Time frame: 1 day
Years
Time frame: 1 day
Male or female
Time frame: 1 day
Yes or No
Time frame: 1 day
Yes or No
Time frame: 1 day
Weight/(size)2 expressed in in kg/m^2
Time frame: 1 day
Yes or No
Time frame: 30 days
Number of patients with at least one pulmonary infection within 21-30 days after EUS-FNA
Contact information is provided by the study sponsor or research team.
Société Française d'Endoscopie Digestive
Other
Prevention of Infection After EUS-FNA of Pancreatic Cystic Lesions: A French Multicenter Prospective Comparative Observational Study
Acronym: PrePaCyst
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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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