Nordic Pancreatic Cancer Trial (NorPACT) - 1

NCT02919787 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 140

Last updated 2024-11-20

No results posted yet for this study

Summary

This study evaluate the additional effect of adding chemotherapy prior to resection of a pancreatic head malignancy. The patients will be randomized into two groups; surgery first (control group) and neoadjuvant chemotherapy (intervention). Primary endpoint is overall survival after resection

Conditions

Interventions

DRUG

5-FU

Neoadjuvant treatment

DRUG

Oxaliplatine

Neoadjuvant treatment

DRUG

Irinotecan

Neoadjuvant treatment

PROCEDURE

Pancreatic surgery

All patients

DRUG

5-FU

Adjuvant treatment

DRUG

Oxaliplatine

Adjuvant treatment

DRUG

Irinotecan

Adjuvant treatment

Sponsors & Collaborators

  • St. Olavs Hospital

    collaborator OTHER
  • Haukeland University Hospital

    collaborator OTHER
  • University Hospital of North Norway

    collaborator OTHER
  • Sahlgrenska University Hospital

    collaborator OTHER
  • Karolinska University Hospital

    collaborator OTHER
  • University Hospital, Linkoeping

    collaborator OTHER
  • Lund University Hospital

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • Helsinki University Hospital, Finland

    collaborator UNKNOWN
  • Norrlands University Hospital

    collaborator OTHER
  • Helse Stavanger HF

    collaborator OTHER_GOV
  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Knut Jorgen Labori, MD PhD · Oslo University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2022-12-22
Completion
2026-04-30

Countries

  • Denmark
  • Finland
  • Norway
  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02919787 on ClinicalTrials.gov