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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02857413
Other study ID # P/2015/281
Secondary ID
Status Completed
Phase N/A
First received August 2, 2016
Last updated August 4, 2016
Start date January 2016
Est. completion date July 2016

Study information

Verified date August 2016
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial Summary

The aim of this study is the evaluation of the frequency of xerostomia and their management after radiotherapy in head and neck cancer.

The quality of life of these patients is also analysed with European Organization for Research and Treatment of Cancer Quality of life Questionnaire H&N35 (EORTC QLQ H&N35).


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date July 2016
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- patient with head and neck cancer after radiotherapy treatment

Exclusion Criteria:

- patient already treated for xerostomia for other reason : Sjögren's syndrome, medication, diabetes,...

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU Besançon Besançon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of xerostomia and their management after radiotherapy in head and neck cancer patients describe the severity of their xerostomia and their management in a standardized questionnaire at enrollment No
Secondary quality of life af patients after radiotherapy in head and neck cancer patients describe their quality of life in a standardized questionnaire at enrollment No
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