- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01989624
PAncreatic Adenocarcinoma in Hospital (APACH)
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.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Jolimont, Belgium
- CH de Jolimont
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Aix en Provence, France, 13616
- CHIAP
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Angoulême, France
- CH Angoulême
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Aubenas, France, 07200
- CH d'Aubenas
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Auch, France, 32008
- CH Auch
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Aulnay sous bois, France
- CH Robert Ballanger
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Avignon, France
- Ch Avignon
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Bagnols sur Ceze, France
- CH Bagnols sur Ceze
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Bayeux, France, 14400
- Ch Bayeux
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Blois, France, 41016
- CH BLOIS
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Bourg en Bresse, France
- CH Bourg en Bresse
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Bourges, France, 18000
- CH de Bourges
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Bressuire, France
- CH Nord Deux Sèvres
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Bry sur Marne, France
- CH Saint Camille
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Béziers, France, 34500
- CH Beziers
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Castres, France, 81108
- HPA Castres Mazamet
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Chalons en champagne, France
- CH Chalons En Champagne
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Chambery, France
- CH Chambery
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Chartres, France, 28630
- CH Chartres
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Cholet, France
- Ch Cholet
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Château Gontier, France
- CH Haut Anjou
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Châteauroux, France, 36000
- Ch Chateauroux
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Compiègne, France
- CH Compiègne Noyon
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Corbeil Essonnes, France
- CH SUd Francilien
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Creil, France, 60109
- CH de Creil
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Créteil, France, 94000
- CHI Creteil
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Dourdan, France
- CH Dourdan
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Draguignan, France
- CH Draguignan
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Dreux, France, 28100
- CH Dreux
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Eaubonne, France, 95600
- CH Simone VEIL
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Ferolles, France
- CH Forcilles
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Gap, France
- CHICAS
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Gonesse, France, 95500
- CH Gonesse
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La Roche sur Yon, France, 85925
- Centre Hospitalier Départemental Vendée
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Lagny sur Marne, France, 77400
- Centre Hospitalier de Lagny
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Le Mans, France
- CH du Mans
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Lens, France
- Lens
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Les Sables d'Olonne, France, 85100
- Centre Hospitalier Côté de lumière
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Macon, France
- Hôpital des chanaux
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Meaux, France, 77100
- Centre Hospitalier de Meaux
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Melun, France
- CH Melun
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Metz, France
- CHR de Mercy-Metz
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Montargis, France, 45207
- CHAM
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Montauban, France
- CH Montauban
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Montelimar, France, 26200
- Centre Hospitalier Montelimar
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Montfermeil, France
- Ch Montfermeil
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Niort, France
- CH Niort
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Oloron Sainte Marie, France
- CHG Oloron
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Orléans, France, 45000
- CHR Orleans
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Pau, France
- CH Francois Mitterand
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Perpignan, France, 66046
- Centre Hospitalier de Perpignan
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Poissy, France, 78600
- CHI Poissy Saint Germain
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Pontoise, France
- CH Pontoise
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Pringy, France, 74374
- CH de la Region d'Annecy
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Quimper, France, 29107
- CH Quimper
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Roubaix, France
- CH Roubaix
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Saint Brieuc, France, 22200
- Centre Hospitalier Yves Le Foll
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Saint Quentin, France
- CH Saint Quentin
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Saint-Denis, France
- CH de la Fontaine
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Tarbes, France, 65013
- Centre Hospitalier de Bigorre
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Toulon, France
- CH Sainte Musse
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Tourcoing, France
- Ch Tourcoing
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Valenciennes, France
- CH Valenciennes
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Vannes, France, 56017
- CHBA de Vannes
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Villeneuve Saint-Georges, France, 94190
- CHIV Villeneuve Saint-Georges
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La Réunion
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Saint-Paul, La Réunion, France, 97866
- CH Gabriel Martin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Living in France
- Pancreatic adenocarcinoma histologically or cytologically proven
- primary diagnosis
- Agreed to participate
Exclusion Criteria:
- Suspected pancreatic adenocarcinoma histologically or cytologically unproven
- Refused to participate
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Pancreatic Adenocarcinoma
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Survival
Time Frame: patient death (following during 5 year)
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patient death (following during 5 year)
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Collaborators and Investigators
Investigators
- Principal Investigator: Roger FAROUX, PH, Centre Hospitalier Départemental Vendée
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHD064-13
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Memorial Sloan Kettering Cancer CenterRecruitingPancreatic Cancer | Pancreatic Cancer Metastatic | Pancreatic Cancer Stage IV | Metastatic Pancreatic Carcinoma | Metastatic Pancreatic Adenocarcinoma | Pancreatic Carcinoma | Metastatic Pancreatic Cancer | Pancreatic Cancer Non-resectable | Metastatic Pancreatic Ductal Adenocarcinoma | Pancreatic Carcinoma... and other conditionsUnited States
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Jean-Luc Van LaethemCelgene CorporationCompletedPancreatic Adenocarcinoma Resectable | Pancreatic Adenocarcinoma Metastatic | Pancreatic Adenocarcinoma Locally AdvancedBelgium