Oral Health in Patients With Severe Eating Disorders An Interview, Questionnaire and Intervention Study With a Focus on Quality of Life

Status: Recruiting
Location: See location...
Intervention Type: Other, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The overall aim of the research project is to assess whether the quality of life of patients with severe eating disorders is improved by dental treatment. Patients diagnosed with anorexia nervosa, bulimia nervosa or non-specific binge eating disorder with extensive dental treatment need will be treated with resin composite restorations or prosthetic therapy. The primary outcome measures is oral health related quality of life. Secondary are orofacial functions and oral esthetics. Patients will be compared to a waiting list.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: f
View:

• Patients diagnosed with anorexia nervosa, bulimia nervosa or non-specific binge eating disorder for a minimum of 10 years = definition of a severe eating disorder where extensive dental damage can be anticipated to find.

• Need of dental treatment of at least six teeth in one jaw,

Locations
Other Locations
Sweden
Eastman Dental Institute
RECRUITING
Stockholm
Contact Information
Primary
Ulrica Gidlund, DDS
ulrica.gidlund@ki.se
+46735089213
Backup
Goran Dahllof, PhD
goran.dahllof@ki.se
+46706479733
Time Frame
Start Date: 2022-12-27
Estimated Completion Date: 2027-11-15
Participants
Target number of participants: 90
Treatments
Experimental: Oral rehabilitation
Name Oral rehabilitation. Patients receiving dental treatment will be allocated to one of two different treatment groups based on individual treatment need and proven experience. Patients in group 1 will be treated with minimal invasive treatment, with restorative composite fillings. Patients in group 2 will be treated with prosthetic rehabilitation, dental crowns.
Other: Waiting list
Name: Waiting list. Patients in waiting list will receive no treatment. After four months they will be offered to be included in the oral rehabilitation arm.
Related Therapeutic Areas
Sponsors
Leads: Karolinska Institutet
Collaborators: Public Dental Health Service in Stockholm AB

This content was sourced from clinicaltrials.gov