CClinicalTrials.gg
CompletedNCT01989624APACHUpdated Mar 14, 2022

PAncreatic Adenocarcinoma in Hospital

An observational study in Pancreatic Adenocarcinoma, sponsored by Centre Hospitalier Departemental Vendee. Completed at 66 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-03-14.

Sponsored by Centre Hospitalier Departemental Vendee · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,204
Ages
18 Years and older
Sex
All
01

Study summary

Few data are currently available in the literature on pancreatic adenocarcinoma in France. About 8,000 new cases each year in France. The 5-year survival for all stages combined is \<5%. This is the only digestive cancer in which mortality / incidence ratio is 98%.

Epidemiological characteristics at diagnosis, the impact on the survival of recent advances related to surgery, adjuvant chemotherapy and new standard forms of adjuvant chemotherapy (FOLFIRINOX) are mispriced in real life.

The development of new drugs and the development of Phase II and III require a better understanding of the state of this disease in the country.

The main objective is to describe the characteristics of the pancreatic adenocarcinoma at diagnosis in France and make an inventory of diagnostic practices and support.

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Conditions studied

  • Pancreatic Adenocarcinoma

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Keywords

  • Pancreatic adenocarcinoma
  • diagnosis
  • treatment
03

In context

Adenocarcinoma

2,004 studies on the registry are indexed under Adenocarcinoma; 375 are open to participants now.

This study's enrollment of 1,204 is above the median of 153 across 332 observational studies indexed under Adenocarcinoma.

Browse Adenocarcinoma studies →

Lead sponsor

Centre Hospitalier Departemental Vendee is the lead sponsor of 81 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patient in hepatogastroenterology in general hospital

Inclusion criteria

  • Living in France
  • Pancreatic adenocarcinoma histologically or cytologically proven
  • primary diagnosis
  • Agreed to participate

Exclusion criteria

Exclusion Criteria:

  • Suspected pancreatic adenocarcinoma histologically or cytologically unproven
  • Refused to participate
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,204 participants (actual)
Patient registry
No

Groups and cohorts

  • Pancreatic Adenocarcinoma
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What researchers measure

Primary outcomes

  1. Survival

    Time frame: patient death (following during 5 year)

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Study locations

66 sites
  • CH de Jolimont
    Jolimont, Belgium
  • CH Gabriel Martin
    Saint-Paul, La Réunion 97866, France
  • CHIAP
    Aix en Provence, 13616, France
  • CH Angoulême
    Angoulême, France
  • CH d'Aubenas
    Aubenas, 07200, France
  • CH Auch
    Auch, 32008, France
  • CH Robert Ballanger
    Aulnay sous bois, France
  • CH Avignon
    Avignon, France
  • CH Bagnols sur Ceze
    Bagnols sur Ceze, France
  • CH Bayeux
    Bayeux, 14400, France
  • CH Blois
    Blois, 41016, France
  • CH Bourg en Bresse
    Bourg en Bresse, France
  • CH de Bourges
    Bourges, 18000, France
  • CH Nord Deux Sèvres
    Bressuire, France
  • CH Saint Camille
    Bry sur Marne, France
  • CH Béziers
    Béziers, 34500, France
  • HPA Castres Mazamet
    Castres, 81108, France
  • CH Chalons en champagne
    Chalons en champagne, France
  • CH Chambery
    Chambery, France
  • CH Chartres
    Chartres, 28630, France
  • Ch Cholet
    Cholet, France
  • CH Haut Anjou
    Château Gontier, France
  • CH Châteauroux
    Châteauroux, 36000, France
  • CH Compiègne Noyon
    Compiègne, France
  • CH sud francilien
    Corbeil Essonnes, France
  • CH de Creil
    Creil, 60109, France
  • CHI Créteil
    Créteil, 94000, France
  • CH Dourdan
    Dourdan, France
  • CH Draguignan
    Draguignan, France
  • CH Dreux
    Dreux, 28100, France
  • CH Simone Veil
    Eaubonne, 95600, France
  • CH Forcilles
    Ferolles, France
  • Chicas
    Gap, France
  • CH Gonesse
    Gonesse, 95500, France
  • Centre hospitalier départemental Vendée
    La Roche sur Yon, 85925, France
  • Centre Hospitalier de Lagny
    Lagny sur Marne, 77400, France
  • CH du Mans
    Le Mans, France
  • Lens
    Lens, France
  • Centre Hospitalier Côté de lumière
    Les Sables d'Olonne, 85100, France
  • Hôpital des chanaux
    Macon, France
  • Centre Hospitalier de Meaux
    Meaux, 77100, France
  • CH Melun
    Melun, France
  • CHR de Mercy-Metz
    Metz, France
  • CHAM
    Montargis, 45207, France
  • CH Montauban
    Montauban, France
  • Centre Hospitalier Montelimar
    Montelimar, 26200, France
  • CH Montfermeil
    Montfermeil, France
  • CH Niort
    Niort, France
  • CHG Oloron
    Oloron Sainte Marie, France
  • CHR Orléans
    Orléans, 45000, France
  • CH François Mitterand
    Pau, France
  • Centre Hospitalier de Perpignan
    Perpignan, 66046, France
  • CHI Poissy Saint Germain
    Poissy, 78600, France
  • CH Pontoise
    Pontoise, France
  • CH de la région d'Annecy
    Pringy, 74374, France
  • CH Quimper
    Quimper, 29107, France
  • CH Roubaix
    Roubaix, France
  • Centre hospitalier Yves Le Foll
    Saint Brieuc, 22200, France
  • CH Saint Quentin
    Saint Quentin, France
  • CH de la Fontaine
    Saint-Denis, France
  • Centre Hospitalier de Bigorre
    Tarbes, 65013, France
  • CH Sainte Musse
    Toulon, France
  • CH Tourcoing
    Tourcoing, France
  • CH Valenciennes
    Valenciennes, France
  • CHBA de Vannes
    Vannes, 56017, France
  • CHIV Villeneuve Saint-Georges
    Villeneuve Saint-Georges, 94190, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 14, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01989624
Lead sponsor
Centre Hospitalier Departemental Vendee
Responsible party
Sponsor
First posted
Nov 21, 2013
Start date
Oct 18, 2013
Primary completion
Dec 4, 2015
Completion
Dec 2020
Last update
Mar 14, 2022

Study contacts

Roger FAROUX, PH
principal investigator · Centre hospitalier départemental Vendée

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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