Survey on Oral Health in Cystic Fibrosis Patients
Oral Health Status of Cystic Fibrosis Patients. An Online Survey in Collaboration With the Vaincre la Mucoviscidose Patient Association.
This study is trying to understand how cystic fibrosis affects oral health and quality of life for adults by asking them about their dental experiences through an online survey.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Ivry-sur-Seine, Île-de-France Region) |
| Trial ID | NCT06356246 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the oral health status and quality of life of adult patients with cystic fibrosis (CF) through an online survey. It focuses on understanding the relationship between CF and oral health issues, including periodontal disease and oral hygiene habits. The study seeks to gather data from CF patients to identify potential oral health challenges as the population ages and life expectancy increases. By utilizing the OHIP-14 questionnaire, the study will evaluate the impact of oral health on the quality of life for these patients.
Who should consider this trial
Good fit: Ideal candidates for this study are adult cystic fibrosis patients over the age of 18 who are fluent in French.
Not a fit: Patients who are under 18 years old or do not speak French may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of oral health challenges in cystic fibrosis patients, leading to improved dental care strategies.
How similar studies have performed: While studies have explored oral health in CF, this approach focusing on adults is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adult patient (\> 18 years old) 2. Cystic fibrosis patient 3. Patient who speaks and understands French well enough to read and understand the study information leaflet. 4. Patient does not object to participation in the study Exclusion Criteria: NA
Where this trial is running
Ivry-sur-Seine, Île-de-France Region
- Marjolaine GOSSET — Ivry-sur-Seine, Île-de-France Region, France (Recruiting)
Study contacts
- Study coordinator: Marjolaine GOSSET, MD, PhD
- Email: marjolaine.gosset@aphp.fr
- Phone: +33 (0)1 49 59 48 20
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.