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NCT Number: NCT02501174

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

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.

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Key information

Conditions

Cancer Neoplasms

Age range

65 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier d'Arras, Arras, France

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  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 outcomes

  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

Sponsors and collaborators

Lead sponsor

Centre Oscar Lambret

Other

Registry information

Acronym: CONSOG

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Jul 17, 2015
Registry last updated
Mar 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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