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Trial Radar IA
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Impact of GLP-1 Receptor Agonists on Patients With IPMN (IPMN-GLP1RA) 30

Non ancora in arruolamento
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La sperimentazione clinica NCT07014709 (IPMN-GLP1RA) è uno studio osservazionale per IPMN (Neoplasia Mucinosa Papillare Intraduttale), IPMN pancreatica, GLP-1, Neoplasia mucinosa papillare intraduttale del pancreas, Glucagon-Like Peptide-1 Receptor Agonists, attualmente non ancora in arruolamento. L'arruolamento dovrebbe iniziare il 31 maggio 2025, con l'obiettivo di raggiungere 30 partecipanti. Sotto la guida di Hôpital Fribourgeois, dovrebbe concludersi entro il 31 ottobre 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 11 giugno 2025.
Sommario breve
This study investigates the impact of GLP-1 receptor agonists (GLP-1 RAs) on patients with intraductal papillary mucinous neoplasms (IPMNs), a type of pancreatic cystic neoplasm that can progress to malignancy. With the increasing use of GLP-1 RAs for managing diabetes and obesity, concerns about their potential to influence pancreatic conditions, like IPMNs, have emerged. Although GLP-1 RAs are generally safe, their...Mostra di più
Descrizione dettagliata
This is a retrospective, multicentric cohort study designed to investigate the impact of GLP-1 receptor agonists (GLP-1 RAs) on patients with intraductal papillary mucinous neoplasms (IPMNs), a subtype of pancreatic cystic neoplasms with variable but potentially significant malignant potential. IPMNs are increasingly diagnosed due to advancements in cross-sectional imaging techniques, and their management often inclu...Mostra di più
Titolo ufficiale

Impact of GLP-1 Receptor Agonists on Patients With Intraductal Papillary Mucinous Neoplasms: A Retrospective Multicentric Cohort Study

Patologie
IPMN (Neoplasia Mucinosa Papillare Intraduttale)IPMN pancreaticaGLP-1Neoplasia mucinosa papillare intraduttale del pancreasGlucagon-Like Peptide-1 Receptor Agonists
Pubblicazioni
Articoli scientifici e documenti di ricerca pubblicati su questo studio clinico:
Altri ID dello studio
  • IPMN-GLP1RA
Numero NCT
Data di inizio (effettiva)
2025-05-31
Ultimo aggiornamento pubblicato
2025-06-11
Data di completamento (stimata)
2026-10-31
Arruolamento (previsto)
30
Tipo di studio
Osservazionale
Stato
Non ancora in arruolamento
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
Intraductal Papillary Mucinous Neoplasms
Patients eligible for this study must have a radiological diagnosis of IPMN
GLP1 receptor agonist
Patients must be under GLP1-RA treatment for ether diabetes or obesity
Esito primario
Misure di esitoDescrizione della misuraArco temporale
Radiological changes in pancreatic cyst characteristic as described in the Kyoto 2023 Consensus
Radiological data, including data from MRI scans, will be used to monitor changes in IPMN characteristics. If only CT scans are available, they will also be evaluated, even if this is not the preferred imaging method for IPMN evaluation
during the GLP1 RA treatment
Esito secondario
Misure di esitoDescrizione della misuraArco temporale
Incidence of acute pancreatitis
The incidence of acute pancreatitis under GLP1-RA will be evaluated
during the GLP1 RA treatment
Changes in serum tumor markers, CA19-9 and CEA levels
When already available in routine analyses before and after initiation of GLP-1 RA therapy, tumor markers level will be assessed to detect any changes
during the GLP1 RA treatment
Changes in Endoscopic ultrasonography (EUS) characteristics
Evaluate the changes of morphological IPMN characteristic in endoscopic ultrasonography (EUS)
during the GLP1 RA treatment
Progression of IPMNs to high-grade dysplasia or invasive malignancy in histopathological analysis
Evaluate the progression of IPMNs to high-grade dysplasia or invasive malignancy in histopathological analysis
during the GLP1 RA treatment
Need for surgical intervention
Investigate the need for surgical intervention associated with the introduction of GLP-1 RA treatment
during the GLP1 RA treatment
Changes in IPMN surveillance protocols
Investigate the need for changes in IPMN surveillance protocols associated with GLP-1 RA use.
during the GLP1 RA treatment
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
  • > 18 years old
  • Radiological diagnosis of IPMN
  • Treated with GLP-1 RAs.
  • Patients must have provided prior informed consent for the use of their coded clinical data in research.

  • radiological diagnosis of IPMN is unclear,
  • no documented history of GLP-1 RAs use
  • patients did not provide signed informed consent, or have documented refusal for research.
Hôpital Fribourgeois logoHôpital Fribourgeois
  • Insel Gruppe AG, University Hospital Bern logoInsel Gruppe AG, University Hospital Bern
  • University Hospital, Geneva logoUniversity Hospital, Geneva
Contatti principali dello studio
Contatto: Melissa Lagger, Dipl.med, +41798164051, [email protected]
1 Centri dello studio in 1 paesi
HFR Hopital fribourgeois, Villars-sur-Glâne, 1752, Switzerland
Melissa Lagger, Contatto, +41263062608, [email protected]
Léo Buhler, Prof., Contatto, +41263062510, [email protected]
Michel Adamina, Prof, Investigatore principale