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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02501174
Acronym
CONSOG
Enrollment
2914
Registered
2015-07-17
Start date
2014-10-01
Completion date
2019-09-01
Last updated
2026-03-18

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

Conditions

Cancer

Keywords

Geriatric oncology

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.

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.

Interventions

None listed

Sponsors

Centre Oscar Lambret
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
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)).Up to 5 years

Secondary

MeasureTime frameDescription
Measurement of the prevalence of different medical and social criteria of interest.Up to 5 yearsPatient's life characteristics (place of living, isolation) and the helps set up (presence of a natural caregiver, sources of professional help).
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.Up to 5 years
Percentage of patients included in trials.Up to 5 years
Temporal evolutions of clinical, medical and social characteristics.Up to 5 years

Countries

France

Contacts

PRINCIPAL_INVESTIGATORCédric GAXATTE, MD

CHRU de Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026