Long-Term Periodontal Tissue Changes Associated With Metal-Ceramic Crowns: An 8-Year Split-Mouth Study
NCT07500636 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32
Last updated 2026-04-03
Summary
The goal of this clinical trial is to to evaluate the periodontal condition around metal-ceramic crown. The main question to be answered is: whether the metal-ceramic crown is the cause of gum changes? The study offers to involve patients who receive single metal-ceramic crown and have kept the same tooth intact on the other side of the mouth.
The condition of the gums around the crown will be compared with the corresponding natural teeth on the oposite side of the mouth. Clinical parameters such as plaque accumulation, bleeding on probing, periodontal pocket depth and gingival recession will be evaluated. All procedures are part of routine dental examination.
Participants:
will be invited for gingival examination 3 months after receiving the metal-ceramic crown, will receive a routine hygiene instruction, will be invited for gingival re-examination after 8 years.
Conditions
- Gingival Health
- Metal-Ceramic Restorations
Interventions
- DEVICE
-
Metal-ceramic crown
The preparation and manufacturing of the MC crown was performed following a standardized clinical and laboratory protocol. Final impression was taken with a one-step technique in a standard tray. All crowns were manufactured in the same dental laboratory. The metal frameworks were fabricated in cobalt-chromium using the lost-wax technique and then veneered with ceramic using a layering technique. All restorations were cemented with zinc phosphate cement. The examination was performed under a dental operating light, using a flat-surfaced intra-oral mirror and a dental/periodontal probe. Both the restored tooth (test) and the contralateral natural tooth (control) were examined. Records were made for the gingival condition using the Silness \& Loe gingival index. Gingival pocket depth measured in millimeters, gingival recession was measured as distance in millimeters (mm) from the cementoenamel junction to the gingival margin.
Sponsors & Collaborators
-
Riga Stradins University
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 20 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2015-10-31
- Primary Completion
- 2016-09-30
- Completion
- 2024-09-30
More Related Trials
-
Soft Tissue Response to Different Restorative Materials Used in Implant Dentistry
NCT06554041 ·Status: RECRUITING ·Phase: NA
-
Influence of Implant Crown Transmucosal Contour Design on Soft and Hard Tissue Clinical Outcomes
NCT06185075 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Peri-implant Mucosal Changes Over Time Following Implant Provisional Removal in the Esthetic Zone
NCT06783595 ·Status: RECRUITING
-
L-PRF for Increasing Keratinised Mucosa Around Implants
NCT03190226 ·Status: COMPLETED ·Phase: PHASE4
-
Posterior Implant-Supported Modified Monolithic Zirconia and Metal-Ceramic Single Crowns: 5 Years Study
NCT04355325 ·Status: UNKNOWN ·Phase: NA
-
Dental Hygiene and Peri-Implant Tissues Homeostasis
NCT03384446 ·Status: COMPLETED ·Phase: NA
-
Comparing Stainless Steel Crowns with Prefabricated Resin Crowns in Primary Molar Teeth
NCT06713330 ·Status: RECRUITING ·Phase: NA
-
Properties and Clinical Performance of Zirconia-based Dental Ceramics
NCT00737308 ·Status: COMPLETED ·Phase: NA
-
Analysis of Enamel Wear Against Ceramic Restorations
NCT00223405 ·Status: COMPLETED
-
Outcome Evaluation of Ceramic Crowns Using Two Different Dental Cements
NCT00591942 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Clinical Wear and Surface Roughness of Partial Restorations Produced by Additive and Subtractive Manufacturing Methods: A Split-Mouth Randomized Controlled Clinical Trial
NCT07057401 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
The Impact of Peri-implant Soft Tissue Properties on Patient-reported and Clinically Assessed Outcomes
NCT03396536 ·Status: COMPLETED
-
Resective Surgical Treatment of Peri-implantitis.
NCT04337645 ·Status: UNKNOWN ·Phase: NA
-
Predictive Value of Reduced Keratinized Mucosa on the Secondary Prevention of Peri-implant Mucositis and Periimplantitis in Patients Attending Regular Supportive Peri-implant Care. A Longitudinal Analysis
NCT05804760 ·Status: COMPLETED
-
Cement Excess at Single Implant Crowns Malmö/Lund
NCT04015427 ·Status: COMPLETED ·Phase: NA
-
Influence of Implant Component Materials on Peri-implant Soft Tissue Horst Response.
NCT05843526 ·Status: COMPLETED ·Phase: NA
-
Minimally Invasive Treatment of Worn Dentition With Innovative CAD-CAM Composites
NCT02828696 ·Status: UNKNOWN ·Phase: NA
-
Healing of Bone/Soft Tissue to Different Abutment Biomaterials and the Impact on Marginal Bone Loss
NCT01961635 ·Status: COMPLETED ·Phase: NA
-
A Prospective Clinical Trial Evaluating Outcomes of Surveyed Zirconia Crowns
NCT06564337 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Cellular and Molecular Inflammatory Mechanisms Leading to Bone Resorption in Peri-implantitis Vs Periodontitis
NCT02664675 ·Status: COMPLETED
-
Zirconia Implants for Replacement of a Single Tooth
NCT04695899 ·Status: ACTIVE_NOT_RECRUITING
-
Evaluation of Implantoplasty in the Treatment of Peri-Implantitis.
NCT06884475 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Influence of Gum Disease Treatment on Long-term Dental Implant Success
NCT03841656 ·Status: UNKNOWN
-
Regenerative Treatment of Peri-implantitis
NCT06153212 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Comparison of Marginal Fit and Internal Adaptation in All-Metal Crowns: an in Vitro Experimental Trial
NCT06067945 ·Status: RECRUITING