Ignite Creation Date:
2024-05-06 @ 8:00 PM
Last Modification Date:
2024-10-26 @ 3:18 PM
Study NCT ID:
NCT06214000
Status:
COMPLETED
Last Update Posted:
2024-03-13
First Post:
2023-12-11
Brief Title:
Primary Care-Based Follow-up of Cancer Survivors of the Prostate and Kidney
Sponsor:
University Hospital Strasbourg France
Organization:
University Hospital Strasbourg France
Study Overview
Official Title:
Primary Care-Based Follow-up of Cancer Survivors of the Prostate and Kidney A Retrospective Study
Status:
COMPLETED
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
LiVHOU
Brief Summary:
In France the second cancer plan of 2009-2013 aimed to strengthen the role of MT by putting it back at the center of patient monitoring in particular by asking regional health agencies to encourage and support local experiments which aim for better coordination between the city and the hospital The third cancer plan for 2014-2019 insists on this measure because it had proven to be unproductive and recommends in addition to the creation of a nurse dedicated to the coordination of care between community medicine and the hospital the creation of a direct telephone line to reach the hospital medical team This measure is mainly aimed at the follow-up of certain cancers that do not require the technical support of the hospital as is the case in the post-operative follow-up of RCC and CaP where the additional examinations carried out during follow-up are carried out in the city
The research hypothesis is that this new method of monitoring had a positive impact on care in terms of quality accessibility organization and costs
The research hypothesis is that this new method of monitoring had a positive impact on care in terms of quality accessibility organization and costs
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None