Skip to main content
OpenTrials
Completed

NCT Number: NCT01797692

Study of Geriatric Patients Aged 75 Years or Older Treated and Cured for Localized Prostate Cancer: Case-control Study

This is a multicenter pilot study, proposed for cases and controls 3 departments in France.

Cases are cured patients who have had prostate cancer for at least 10 years. Cookies are healthy subjects selected by lottery on voter list.

Volunteer subjects (cases and controls) are offered a consultation and assessment with an geriatrician.

Completed

Looking for future studies?

Notify Me

Key information

Age range

75 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Hopitaux universitaires de Strasbourg, Strasbourg, Bas-Rhin, France

Loading trial locations.

About this study

Volunteer subjects (cases and controls) are offered a consultation and assessment with an geriatrician.

During this consultation, ADL, IADL and MMS questionnary will be completed. neurocognitif testing will be done.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

for patients:

  • Patients aged 75 years or more
  • Patients with a personal history of prostate cancer with a diagnosis ≥ 10 years
  • Patients who received curative treatment (surgery, radiotherapy,hormone therapy, brachytherapy, technical ablative) for localized prostate cancer
  • Patients considered cured of prostate cancer (regardless of initial treatment)
  • Patients with previously agreed to participate in a case-control study in the general population (study QALIPRO) as a case and volunteer to receive an assessment of geriatric
  • Signature of consent
  • Affiliation to a social security system

Exclusion criteria

for patients:

  • Patients under 75 years
  • Patients with recurrent or metastatic
  • Persons deprived of liberty or under guardianship

Inclusion criteria

for control population:

  • Male subjects
  • Subjects of 75 years or more
  • Subjects that do not have cancer or a history of cancer (except basal cell skin cancer)
  • Subject has previously agreed to participate in a case-control study in the general population (study QALIPRO) as a voluntary witness and to benefit from a balance oncogeriatrics
  • Subjects who gave their written consent to participate in the study

Treatment and study plan

Geriatric Assessment

Other

A single geriatric assessment with a geriatrician was proposed to patients and to control population.

Primary outcomes

  1. impact of treatments

    Time frame: 10 years after treatment for cancer prostate

    The main objective of this study is to evaluate the impact of treatments and their effects on the autonomy of patients over 75 years have been treated and cured for prostate cancer.

Secondary outcomes

  1. Evaluate the anxiety of patients and controls

    Time frame: 10 years after treatment for cancer prostate

    Evaluate the anxiety of patients and controls

  2. Assessing depression patients and controls

    Time frame: 10 years after treatments for cancer prostate

    Assessing depression patients and controls

  3. Assess the nutritional status of patients and controls

    Time frame: 10 years after treatments for cancer prostate

    Assess the nutritional status of patients and controls

Sponsors and collaborators

Lead sponsor

Centre Francois Baclesse

Other

Registry information

Acronym: PROGE

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Feb 22, 2013
Registry last updated
Mar 4, 2015

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.