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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04704817
Other study ID # CHIRCOLREC-IPC 2018-017
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2021
Est. completion date December 2071

Study information

Verified date January 2021
Source Institut Paoli-Calmettes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Colorectal cancer is the third most common cancer in men, after prostate and lung cancer. It represents 11.2% of all new cases of male cancer. In women, this cancer is the second most common after breast cancer (11.3% of all new cases of female cancer).


Description:

Colorectal cancer is the second leading cause of cancer death in France. It accounts for nearly 12% of all cancer deaths, especially among those 65 and over. However, mortality has declined steadily since 1980. Access to screening for colorectal cancer and resection of precancerous lesions partly explains this decline. All sexes combined, it is estimated that about one in five colorectal cancer is diagnosed at a limited local stage. The treatment is then less heavy and gives better results. With the development of Enhanced Recovery After Surgery (ERAS) protocols and their extension to rectal excision, it becomes imperative to be able to collect operative data from these patients on a perennial basis for the purpose of evaluating our results. Finally, the evaluations resulting from this database could have prognostic value and ultimately allow us to adapt the surgical management of the patient according to the results.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1000
Est. completion date December 2071
Est. primary completion date March 2051
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients treated for colonic and / or rectal resection in the oncological digestive surgery department of the Paoli-Calmettes Institute, 2. Patients over 18 years old, 3. Affiliation to a social security scheme, or beneficiary of such a scheme.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
obsevation
prospective data collection for colonic or rectal surgery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Institut Paoli-Calmettes

Outcome

Type Measure Description Time frame Safety issue
Primary clinical events to asses postoperative effects of colonic or rectal excision by collecting clinical events 5 years
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