Actively Recruiting
Supplementary Implants Supporting Conventional Removable Dental Prosthesis (RDPs) in Kennedy Class I
Led by University Hospital, Basel, Switzerland · Updated on 2025-05-11
12
Participants Needed
1
Research Sites
312 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Basel, Switzerland
Lead Sponsor
I
ITI International Team for Implantology, Switzerland
Collaborating Sponsor
AI-Summary
What this Trial Is About
In this study the additional effect of supplementary implants in patients with Kennedy Class I in terms of patient-reported outcome measures (PROMs) and cost-benefit-analyses comparing costs of maintenance care will be investigated
CONDITIONS
Official Title
Supplementary Implants Supporting Conventional Removable Dental Prosthesis (RDPs) in Kennedy Class I
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Voluntarily signed informed consent and willing to attend scheduled follow-up visits
- Male or female aged 18 years or older
- Bilateral missing back teeth behind remaining natural teeth (Kennedy Class I) in upper or lower jaw
- Remaining last natural tooth is a first premolar, canine, or incisor
You will not qualify if you...
- Uncontrolled systemic disease interfering with dental implant therapy
- Smoking more than 10 cigarettes or tobacco equivalents per day
- Alcohol or drug abuse
- Chronic pain
- Untreated periodontitis or poor oral hygiene (Plaque Index less than 30%)
- Medical condition requiring chronic high-dose steroid or anti-resorptive treatment
- Any condition preventing study completion or affecting result analysis, including history of non-compliance or unreliability
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Reconstructive Dentistry, University Center for Dental Medicine Basel UZB, University of Basel
Basel, Switzerland, 4058
Actively Recruiting
Research Team
N
Nicola Zitzmann, Prof. Dr.
CONTACT
T
Tim Joda, Prof. Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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