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NCT Number: NCT07418164

Endoscopic Management of Biliopancreatic Disease in the Lombardy Pancreas Units

The GENTLENESS study is a prospective, multicenter, observational registry designed to evaluate the endoscopic management of patients with suspected biliopancreatic and periampullary neoplastic diseases within the Pancreas Units network of the Lombardy Region.

Patients undergoing endoscopic ultrasound (EUS) for suspected pancreatic or periampullary malignancies, including pancreatic ductal adenocarcinoma, pancreatic neuroendocrine tumors, cystic pancreatic neoplasms requiring endoscopic, surgical, or oncological management, and periampullary tumors of the distal bile duct, ampulla, or duodenum, will be prospectively enrolled according to standard clinical practice.

The study aims to assess the diagnostic accuracy of EUS-guided tissue acquisition, procedural safety, the need for repeat sampling, and organizational performance indicators, including time to definitive cyto-histological diagnosis and time to initiation of disease-specific treatment. No additional procedures beyond routine clinical care will be performed as a result of study participation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

ASST Papa Giovanni XXIII - P.O. Papa Giovanni XXIII Bergamo, Bergamo, Italy

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About this study

Despite advances in oncological therapies, pancreatic cancer remains one of the leading causes of cancer-related mortality worldwide, with an increasing burden projected over the coming decades. The diagnostic and therapeutic pathway of biliopancreatic malignancies is complex and requires a high level of multidisciplinary expertise, particularly in high-volume referral centers organized as Pancreas Units.

Endoscopic ultrasound (EUS) plays a central role in the diagnostic work-up of biliopancreatic and periampullary lesions, allowing high-resolution morphological assessment and, when indicated, tissue acquisition through fine-needle aspiration (FNA) or fine-needle biopsy (FNB). Accurate histological diagnosis is essential for therapeutic decision-making, including surgical planning, systemic therapy, and molecular profiling.

The Lombardy Region has adopted a Hub-and-Spoke organizational model for Pancreas Units, defining minimum procedural volumes, expertise requirements, and performance benchmarks for referral centers. However, a centralized prospective system for monitoring endoscopic activity, diagnostic performance, and procedural outcomes across these centers is currently lacking.

The GENTLENESS study has been designed to prospectively collect real-world data on EUS procedures performed in Lombardy Pancreas Unit Hub centers, with the primary objective of evaluating the diagnostic accuracy of EUS-guided biopsies. Secondary objectives include assessment of procedural volume, sampling techniques, need for repeat biopsies, complication rates, and time intervals from procedure to definitive diagnosis and initiation of treatment.

The study is observational, does not introduce changes to clinical practice, and reflects routine patient management pathways. Any future analyses beyond the scope of the present registry will require separate Ethics Committee approval.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (≥18 years)
  • Clinical, biochemical, and/or imaging suspicion of pancreatic neoplasia (adenocarcinoma, neuroendocrine tumors, cystic neoplasms requiring endoscopic, surgical, or oncological treatment) or periampullary neoplasia (distal bile duct, ampulla, duodenum)
  • Candidate for EUS according to standard clinical practice
  • Ability to understand and sign informed consent

Exclusion criteria

  • Age <18 years
  • Pregnancy or breastfeeding
  • Conditions other than those defined in the inclusion criteria
  • Inability to provide informed consent
  • Refusal to participate in the study

Treatment and study plan

Primary outcomes

  1. Diagnostic Accuracy

    Time frame: 30 days

    Number of patients with a correct diagnosis obtained through EUS-guided cyto-histological sampling, confirmed by the final diagnosis

Secondary outcomes

  1. Procedural Volume

    Time frame: 6 months

    Number of EUS procedures performed for suspected biliopancreatic neoplasms

  2. Need of Repeat Sampling

    Time frame: 30 days, 60 days

    Need for additional EUS-guided sampling after an initial non-diagnostic procedure

  3. Sampling Technique

    Time frame: Intraprocedural

    Type of tissue acquisition (FNA vs FNB; ROSE vs MOSE)

  4. Adverse Events

    Time frame: Intraprocedural, 30 days

    Intra- and post-procedural complications classified according to ASGE criteria

  5. Time to Diagnosis

    Time frame: 30 days, 60 days

    Time from EUS to availability of definitive cyto-histological report

  6. Time to Treatment

    Time frame: 30 days, 60 days

    Time from diagnosis to initiation of disease-specific treatment

Study contacts

Contact information is provided by the study sponsor or research team.

Gaetano Lauri, PhDs

CONTACT

[email protected]

0226436303

Laura Apadula, MSN

CONTACT

[email protected]

0226433979

Sponsors and collaborators

Lead sponsor

IRCCS San Raffaele

Other

Registry information

Official study title

Endoscopic Management of Suspected Biliopancreatic Disease Within the Lombardy Pancreas Units: a Prospective Observational Study

Acronym: GENTLENESS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 18, 2026
Registry last updated
Feb 18, 2026

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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