Characteristics of a Maxillofacial Prosthesis Consultation Within Assistance Publique - Hopitaux de Paris (PEC-PMF)
Primary Purpose
Head and Neck Neoplasm, Cleft Palate, Cleft Lip
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Questionnaire
Sponsored by
About this trial
This is an interventional other trial for Head and Neck Neoplasm focused on measuring Head and Neck neoplasm, cleft, maxillofacial prosthesis
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years old
- Patients consulting for Maxillofacial Prosthesis management (Dental Department, Pitié-Salpêtrière Hospital Group)
- Information and collection of the patient's non-opposition to participation in the research
- Good written and oral comprehension of the French language
Exclusion Criteria:
- Under guardianship or curatorship
- Cognitive disorders: confounding, impaired memory, attention, reasoning and/or judgment
Sites / Locations
- Assistance Publique - Hôpitaux de Paris
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Patients treated in the MaxilloFacial Prosthesis consultation
Arm Description
Patients treated in the MaxilloFacial Prosthesis consultation (Dental Department, Pitié-Salpêtrière Hospital Group)
Outcomes
Primary Outcome Measures
Measurement of the prevalence of socio-demographic and medical characteristics of consulting patients in the consultation of Maxillofacial Prosthesis
Characteristics such as age, gender, medical history, dental history, oral hygiene will be collected.
Secondary Outcome Measures
Measurement of overall quality of life: Questionnaire WHOQOL-BREF
Questionnaire WHOQOL-BREF (World Health Organization Quality of Life) - 26 items rated on a 5 point likert scale (low score of 1 to high score of 5)
Measurement of quality of life related to oral health: Questionnaire GOHAI
Questionnaire GOHAI (General Oral Health Assessment Index) 12 items rated on a 5 point likert scale (low score of 1 to high score of 5)
Correlation between quality of life and clinical factors
Medical factors will be collected such as :
Drug consumption (number of drugs taken per day)
Disorders associated with substance loss (number of disorders)
Reconstructive surgery (presence or absence)
Oral opening limitation (height in millimeters)
Full Information
NCT ID
NCT04277273
First Posted
December 12, 2019
Last Updated
January 27, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT04277273
Brief Title
Characteristics of a Maxillofacial Prosthesis Consultation Within Assistance Publique - Hopitaux de Paris
Acronym
PEC-PMF
Official Title
Descriptive Epidemiological Study of Maxillofacial Prosthesis Consultation at Groupe Hospitalier Pitié-Salpêtrière for Sociodemographic, Medical Characteristics and Quality of Life
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
November 13, 2020 (Actual)
Primary Completion Date
May 7, 2021 (Actual)
Study Completion Date
May 7, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients treated with Maxillofacial Prosthesis have loss of maxillary and/or mandibular substances. Few data are available on quality of life of these patients and its association with some of their socio-demographic, medical and clinical characteristics.
Detailed Description
Patients treated with Maxillofacial Prosthesis have loss of maxillary and/or mandibular substances (oral-nasal or oral-sinusal communication, removal of the soft palate, removal of part of the lower jaw). These losses are mainly due to the surgical consequences of cancers of the upper aerodigestive tract, trauma or sequelae of labio-palate clefts. Depending on the etiology of substance loss, there are 3 main therapeutics: surgical approach, radiotherapy and chemotherapy. The effects of these treatments are functional, aesthetic and psychological. The functions impacted are chewing, phonation, ventilation and swallowing.
Few data are available on quality of life of these patients and its association with some of their socio-demographic, medical and clinical characteristics (drug use, type of maxillo-mandibular loss of substance, disorder(s) associated with substance loss, ...).
This study investigates the socio-demographic, medical and quality of life characteristics of Maxillofacial Prosthesis consultation's patients (Department of Dentistry, GHPS) and the potential associations between quality of life and some of these characteristics.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Neoplasm, Cleft Palate, Cleft Lip
Keywords
Head and Neck neoplasm, cleft, maxillofacial prosthesis
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
83 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients treated in the MaxilloFacial Prosthesis consultation
Arm Type
Other
Arm Description
Patients treated in the MaxilloFacial Prosthesis consultation (Dental Department, Pitié-Salpêtrière Hospital Group)
Intervention Type
Other
Intervention Name(s)
Questionnaire
Intervention Description
Questionnaires WHOQOL-BREF and GOHAI
Primary Outcome Measure Information:
Title
Measurement of the prevalence of socio-demographic and medical characteristics of consulting patients in the consultation of Maxillofacial Prosthesis
Description
Characteristics such as age, gender, medical history, dental history, oral hygiene will be collected.
Time Frame
During the consultation (Day 1)
Secondary Outcome Measure Information:
Title
Measurement of overall quality of life: Questionnaire WHOQOL-BREF
Description
Questionnaire WHOQOL-BREF (World Health Organization Quality of Life) - 26 items rated on a 5 point likert scale (low score of 1 to high score of 5)
Time Frame
During the consultation (Day 1)
Title
Measurement of quality of life related to oral health: Questionnaire GOHAI
Description
Questionnaire GOHAI (General Oral Health Assessment Index) 12 items rated on a 5 point likert scale (low score of 1 to high score of 5)
Time Frame
During the consultation (Day 1)
Title
Correlation between quality of life and clinical factors
Description
Medical factors will be collected such as :
Drug consumption (number of drugs taken per day)
Disorders associated with substance loss (number of disorders)
Reconstructive surgery (presence or absence)
Oral opening limitation (height in millimeters)
Time Frame
During the consultation (Day 1)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years old
Patients consulting for Maxillofacial Prosthesis management (Dental Department, Pitié-Salpêtrière Hospital Group)
Information and collection of the patient's non-opposition to participation in the research
Good written and oral comprehension of the French language
Exclusion Criteria:
Under guardianship or curatorship
Cognitive disorders: confounding, impaired memory, attention, reasoning and/or judgment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin POMES, PH
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Assistance Publique - Hôpitaux de Paris
City
Paris
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Characteristics of a Maxillofacial Prosthesis Consultation Within Assistance Publique - Hopitaux de Paris
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