Skip to content

Estimating the Effects of Neoadjuvant Chemoradiotherapy for Adenocarcinoma of the Pancreatic Head using Inverse Probability of Treatment Weighting: A Dual-institution Observational Study

Estimating the Effects of Neoadjuvant Chemoradiotherapy for Adenocarcinoma of the Pancreatic Head using Inverse Probability of Treatment Weighting: A Dual-institution Observational Study - NACRT for PDAC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019719
Enrollment
504
Registered
2015-11-09
Start date
2015-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Resectable pancreatic adenocarcinoma, borderline resectable pancreatic adenocarcinoma with portal vein invasion or arterial invasion

Interventions

Sponsors

Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Histologically proven pancreatic adenocarcinoma (2) Age between 20 and 85 years (3) ECOG performance status of 0 or 1 (4)Resectable and Borderline resectable pancreatic cancer (NCCN criteria) (5) Adequate hematologic, renal, hepatic and respiratory function (6) Written informed consent (7)Operation performed in Nagoya University Hospital and Kansai Medical University

Exclusion criteria

Exclusion criteria: (1) Unresectable pancreatic cancer (NCCN criteria) (2)Tumors with encasement or stenosis of the arteries, those abutted with the celiac axis (3) Hematologic, renal, hepatic and respiratory dysfunction (4)Active infections (5) Severe cardiac disorder, renal disorder, liver disorder, ulcer with bleeding, intestinal tract paralysis, uncontrollable diabetes mellitus (6) Presence of pleural effusion or ascites requiring drainage (7)Pregnant females or nursing mothers who can not stop lactation. Patients or partners, who don't attempt to doing contraception during the study period. (8) Severe mental disorder (9) Severe drug hypersensitivity (10) As determined by the principal investigator or the sub-investigator the subject is not adequate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Survival, short-term clinic benefit, the effect of NACRT, adverse events

Countries

Japan

Contacts

Public ContactTsutomu Fujii

Nagoya University Graduate School of Medicine Gastroenterological Surgery (Surgery II)

fjt@med.nagoya-u.ac.jp052-744-2245

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026