Rigid Versus Non-Rigid Digitally Fabricated Telescopic Double Crown Prosthesis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Rigid telescopic double crown prosthesis, Non-rigid telescopic double crown prosthesis.
- Who it may be relevant to
- Registry conditions: Tooth Loss and Rehabilitation With Telescopic Crown Prostheses. Basic parameters: 50 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Rigid Versus Non-Rigid Digitally Fabricated Telescopic Double Crown Prosthesis Connecting Teeth and Implants: A Crossover Study of Soft Tissue Health and Patient Satisfaction
Overview
This study aims to compare the clinical and patient satisfaction outcomes of rigid versus non-rigid digitally fabricated telescopic double crown prostheses supported by teeth and implants. The study evaluates the effect of different attachment designs on prosthetic performance and patient satisfaction."
Interventions
- Device Rigid telescopic double crown prosthesis
Digitally fabricated rigid telescopic double crown prosthesis - Device Non-rigid telescopic double crown prosthesis
Digitally fabricated non-rigid telescopic double crown prosthesis
Primary outcome measures
- Soft tissue health [Time frame: Immediately after insertion, 3 months, and 6 months after prosthesis insertion]
Secondary outcome measures (1)
- Patient satisfaction [Time frame: Immediately after insertion, 3 months, and 6 months after prosthesis insertion]
Eligibility criteria
- Inclusion Criteria:
Patients requiring telescopic overdenture prosthesis.
Exclusion criteria
Patients with systemic conditions affecting periodontal or prosthetic treatment.
Patients unable to attend follow-up visits
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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07682623 · TELDC-2025