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Study of Elderly Patients With Cancer and Seen in Consultation of Geriatric Oncology in the Nord Pas-de-Calais (CONSOG).

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02501174
Recruitment Status : Recruiting
First Posted : July 17, 2015
Last Update Posted : July 25, 2019
Sponsor:
Information provided by (Responsible Party):
Centre Oscar Lambret

Brief Summary:
The aim of this study is to establish a common geriatric oncology medical database. The patients concerned are the patients having benefited from a geriatric oncology consultation in one of the participating centres. This database is designed with a view on the one hand to better describe to better understand this population and on the other hand to facilitate the conduct of future retrospective or prospective studies on this population. The constitution of this observatory of patients seen in consultation should facilitate the development of studies from the analysis of data collected, and occasional surveys by the rapid identification of cases. Data from this database could provide clinicians with valuable informative elements of descriptive epidemiology and concerning the organization of care in the geriatric oncology field.

Condition or disease
Cancer

Detailed Description:
The study is presented during the first consultation of oncogeriatric care or after this consultation (for patients having benefited from the consultation between January 2014 and October 2014) : the patient is informed with an information note and is told that he can express its opposition to the use of its clinical data. In case of no opposition from the patient, the referent geriatrician will complete the patient form with the requested data and will forward it for computerized processing.

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Study Type : Observational
Estimated Enrollment : 2500 participants
Observational Model: Case-Only
Time Perspective: Other
Official Title: Study of Elderly Patients With Cancer and Seen in Consultation of Geriatric Oncology in the Nord Pas-de-Calais (CONSOG).
Study Start Date : October 2014
Estimated Primary Completion Date : September 2019
Estimated Study Completion Date : September 2019



Primary Outcome Measures :
  1. Measurement of the prevalence of different clinical criteria of interest : demographic characteristics, disease state, patient status according to the geriatric criteria (Comprehensive Geriatric Assessment (CGA)). [ Time Frame: Up to 5 years ]

Secondary Outcome Measures :
  1. Measurement of the prevalence of different medical and social criteria of interest. [ Time Frame: Up to 5 years ]
    Patient's life characteristics (place of living, isolation) and the helps set up (presence of a natural caregiver, sources of professional help).

  2. Measurement of the association between one or more factors of interest (clinical, biological and medical and social) related to a proposal to amend or not the initially proposed therapeutic strategy. [ Time Frame: Up to 5 years ]
  3. Percentage of patients included in trials. [ Time Frame: Up to 5 years ]
  4. Temporal evolutions of clinical, medical and social characteristics. [ Time Frame: Up to 5 years ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   65 Years and older   (Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients included are patients followed in one of the participating centres and not opposing the use of their medical data.
Criteria

Inclusion Criteria:

  • Patient seen in consultation of geriatric oncology in one of the participating centres in Nord Pas-de-Calais.
  • Age ≥ 65 years
  • Patient having been informed and not opposing the computerized processing of its data.

Exclusion Criteria:

  • Patient having opposed the use of its medical data.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02501174


Contacts
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Contact: Cédric GAXATTE, MD cedric.gaxatte@chru-lille.fr
Contact: Véronique SERVENT, MD v-servent@o-lambret.fr

Locations
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France
Centre Hospitalier d'Arras Recruiting
Arras, France
Contact: Delphine DERVAUX, MD         
Centre Hospitalier Recruiting
Boulogne sur Mer, France, 62200
Contact: Paul TAPIE, MD       p.tapie@ch-boulogne.fr   
Principal Investigator: Paul TAPIE, MD         
Centre Hospitalier Recruiting
Béthune, France, 62408
Contact: Pierre MOITY, MD       pierre.moity@ch-bethune.fr   
Principal Investigator: Pierre MOITY, MD         
Centre Hospitalier, Douai Recruiting
Douai, France
Contact: Delphine DERVAUX, MD         
Centre Hospitalier Recruiting
Dunkerque, France, 59240
Contact: Abdelghani EL AZOUZI, MD       Abdelghani.ElAzouzi@ch-dunkerque.fr   
Principal Investigator: Abdelghani EL AZOUZI, MD         
Hospitalier Le Cateau-Cambresis Recruiting
Le Cateau-Cambrésis, France
Contact: Yann GAUTRET, MD         
CHRU de Lille Recruiting
Lille, France, 59000
Contact: Cédric GAXATTE, MD       cedric.gaxatte@chru-lille.fr   
Principal Investigator: Cédric GAXATTE, MD         
Sub-Investigator: François PUISIEUX, MD         
Sub-Investigator: Marie-Guy DEPUYDT, MD         
Sub-Investigator: Capucine BALDINI, MD         
Hôpital Saint Vincent de Paul Recruiting
Lille, France, 59000
Contact: Virginie BERA, MD       Bera.Virginie@ghicl.net   
Principal Investigator: Virginie BERA, MD         
Centre Oscar Lambret Recruiting
Lille, France, 59020
Contact: Véronique SERVENT, MD       v-servent@o-lambret.fr   
Principal Investigator: Véronique SERVENT, MD         
Sub-Investigator: Marie-Guy DEPUYDT, MD         
Sub-Investigator: Capucine BALDINI, MD         
Polyclinique de Riaumont Recruiting
Liévin, France, 62800
Contact: Rose-Marie DEDEIRE-GAMBIEZ, MD       rmdedeire@ahnac.com   
Principal Investigator: Rose-Marie DEDEIRE-GAMBIEZ, MD         
Hôpital Saint-Philibert Recruiting
Lomme, France, 59160
Contact: Céline DELECLUSE, MD       Delecluse.Celine@ghicl.net   
Principal Investigator: Céline DELECLUSE, MD         
Clinique Saint Jean, Roubaix Recruiting
Roubaix, France
Contact: Virginie BERA, MD         
Centre Hospitalier Recruiting
Tourcoing, France, 59200
Contact: Peggy-Sophie BRZEZINSKI, MD       psbrzezinski@ch-tourcoing.fr   
Principal Investigator: Peggy-Sophie BRZEZINSKI, MD         
Centre de cancérologie Les Dentellières Recruiting
Valenciennes, France, 59300
Contact: Rose-Marie DEDEIRE-GAMBIEZ, MD       rmdedeire@ahnac.com   
Principal Investigator: Rose-Marie DEDEIRE-GAMBIEZ, MD         
Centre Hospitalier Recruiting
Valenciennes, France, 59300
Contact: Anne-Sophie DREUMONT, MD       dreumont-as@ch-valenciennes.fr   
Principal Investigator: Anne-Sophie DREUMONT, MD         
Sub-Investigator: Géraldine GOMMEZ, MD         
Sub-Investigator: Antoine CAILLAU, MD         
Sponsors and Collaborators
Centre Oscar Lambret
Investigators
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Principal Investigator: Cédric GAXATTE, MD CHRU de Lille

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Responsible Party: Centre Oscar Lambret
ClinicalTrials.gov Identifier: NCT02501174    
Other Study ID Numbers: CONSOG-1401
First Posted: July 17, 2015    Key Record Dates
Last Update Posted: July 25, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by Centre Oscar Lambret:
Geriatric oncology
Additional relevant MeSH terms:
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Neoplasms