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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03822988
Other study ID # PSS-2018/PADAONCODERM
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 21, 2019
Est. completion date June 20, 2019

Study information

Verified date January 2019
Source Central Hospital, Nancy, France
Contact Anne-Claire BURSZTEJN
Phone 0383157146
Email ac-bursztejn@chru-nancy.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The law about advance directives is evolving but, in France, few people write it.

Te main endpoint of this research is to estimate the proportion of patients who have written their advance directives or considering doing so in onco-dermatologic population. If this rate remains low, some insights on the reasons will be able to be advanced looking at the point of view and opinion of patients about this topic.

Seconds endpoints are :

For patients against or not planning to write it, understand their reasons

Estimate the proportion of patients requesting information and understand how they would like to receive it.

Investigate a possible association between the stage of the oncological disease and the positioning of the patient concerning advance directives.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date June 20, 2019
Est. primary completion date June 20, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

> 18 ya

With one of the diagnoses below:

- Melanoma

- Skin lymphoma

- Meckel Carcinoma

- localy advanced or metastatic Basal cell carcinoma or squamous cell carcinoma

Exclusion Criteria:

Patients not in possession of all of its cognitive abilities Patients who can't read patients who don't speak french

Study Design


Intervention

Other:
no intervention, only complete a survey
we will ask patients to answer to a survey

Locations

Country Name City State
France CHRU Nancy-Brabois hospital Vandœuvre-lès-Nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Writing by the patient of its advance directives Writing by the patient of his advance directves and, if not writing, positioning of the patient (rather favorable or rather unfavorable) as to the writing of his advance directives. when the patient complete the survey
Secondary reason for not writing advance directives In patients who have not written their advance directives: reason for not writing the advance directives. when the patient complete the survey
Secondary Patient wishing to be more informed about the adavance directives during its management and, if so, by what means. when the patient complete the survey
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