Clinical Evaluation on the Longevity of Glass Ceramic Based Single Tooth Restorations

NCT06898411 | Not Yet Recruiting

• 1 other identifier: OTCS 350528136
• Study Type: observational
• Target: 82
• Locations: 1 country
• Sites: 1

Brief Summary

This retrospective study investigates the longevity of lithium disilicate based glass-ceramic single tooth restorations placed with IPS e.max CAD and IPS e.max Press after a wearing period of more than 15 years. The primary objective is to assess the survival rate of single tooth restorations with IPS e.max CAD and IPS e.max Press after a wearing period of at least 15 years. The secondary objectives are to assess the quality of the single tooth restorations in regard of aesthetic, functional and biological properties.

Conditions

Single Tooth Restoration; Longevity

Keywords

crown; inlay; onlay; glass ceramic; veneer

Outcome Measures

Primary Outcomes (1)

• Survival Rate of single tooth restorations

  Study population recieved single tooth restorations with IPS e.max between 2006-2010. After a wearing time of more than 15 years IPS e.max single tooth restorations were examined by a dentist resulting in survival rates of IPS e.max single tooth restorations after 15 years.

  15 years

Study Arms (1)

Single tooth restoration with IPS e.max

Examination of single tooth restorations with IPS e.max after a wearing time of more than 15 years.

Device: Single tooth restoration with IPS e.max

Interventions

Single tooth restoration with IPS e.max DEVICE

Examination of single tooth restorations with IPS e.max after a wearing time of more than 15 years. Intraoral situation will be examined similar to a standard dental examination while single tooth restorations will be documneted by photos.

Single tooth restoration with IPS e.max

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Adults recieving indirect single tooth restorations (inlay, onlay, veneer or crown) within the internal clinic of Ivoclar Vivadent AG between 2006 and 2010.

You may qualify if:

• Age: \> 18 years
• Informed consent signed and understood by the subject
• Received indirect single tooth restoration (inlay, onlay, veneer or crown) within the internal clinic of Ivoclar Vivadent AG between 2006 and 2010
• Single tooth restoration was done with IPS e.max CAD or IPS e.max Press
• Able to visit the internal clinic of Ivoclar Vivadent AG in Schaan, FL.

You may not qualify if:

• Health status (physical and mental) does not allow participation

Sponsors & Collaborators

• Ivoclar Vivadent AG: lead

Study Sites (1)

Ivoclar Vivadent AG

Schaan, 9494, Liechtenstein

Location

Central Study Contacts

Lukas Enggist, Dr. med. dent.

CONTACT

+423 235 3446; Lukas.Enggist@ivoclar.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 13, 2025
• First Posted: March 27, 2025
• Study Start: April 1, 2025
• Primary Completion: April 30, 2025
• Study Completion: April 30, 2025
• Last Updated: April 2, 2025

Record last verified: 2025-03

Locations

LI (1)