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Clinical Trials in Italy / NCT07241663
Recruiting Observational

Surgery for Locally Unresectable Pancreatic Cancer

NCT07241663 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-01-01
Last updated
2025-11-26

Condition(s) studied

Locally Advanced Pancreatic Adenocarcinoma

Investigational drug(s) / intervention(s)

Questionnaire

Questionnaire: Each enrolled patient will complete quality of life questionnaires, specifically the EORTC QLQ-C30, PAN26, and EQ-5D, at different time points: at enrollment and every 2-3 months after surgery, for up to 2 years.

Study summary

Pancreatic cancer is a severe disease often diagnosed at an advanced stage, when surgery is not possible. New chemotherapy treatments can sometimes shrink the tumor and make surgery an option. This study aims to understand if surgery after such treatments can improve survival and quality of life in selected patients treated at expert centers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients older than 18 years * Patients able to give informed consent * Histologically confirmed pancreatic adenocarcinoma * LAPC stage according to NCCN10 at diagnosis (Figure 1) * Received at least 4 months of induction chemotherapy * RECIST 1.1 stable disease (SD) or partial response (PR) after induction therapy * Patient considered eligible for radical resection by local MDT Exclusion Criteria: * Informed consent withdrawal * Presence of tumor characteristics precluding surgery * Presence of patient significant comorbidities precluding surgery * Unavailable pre-induction therapy abdominal imaging * Pathological confirmation of any tumor different from PDAC

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UOC Chirurgia Generale 2, Azienda Ospedale di Padova, Padova, Italy 35128 Padova Italy Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07241663 on ClinicalTrials.gov ↗ ← All trials in Italy