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NCT05984472: Edelweiss
3-year Clinical Performance of Prefabricated and Composite Veneers
NA trial testing Edelweiss prefabricated veneers in Dental Diseases in 21 participants. Completed in 15 January 2020.
30 December 2019
Quick facts
| Lead sponsor | Ege University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 21 |
| Start date | 15 January 2019 |
| Primary completion | 30 December 2019 |
| Estimated completion | 15 January 2020 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Edelweiss prefabricated veneers
- Ceram-X Duo SphereTec with U-Veneer
Conditions studied
- Dental Diseases — all drugs for Dental Diseases →
- Tooth Discoloration — all drugs for Tooth Discoloration →
Sponsor
Ege University
Who can join
Adults 18 to 60, any sex, with Dental Diseases or Tooth Discoloration. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this study was to evaluate the clinical performances of Edelweiss prefabricated veneers and direct resin composite restorations (Ceram-X Duo SphereTec) performed with U- veneer transparent templates used for anterior diastema closure and tooth reshaping over 3-year. The patient group consisted of individuals who applied for aesthetic complaints on their anterior teeth. 21 volunteer individuals without systemic disease were included in the study. Patients were randomly selected for each group. In Group 1; 38 teeth (10 patients) were restored with Edelweiss prefabricated veneers (Edelweiss Dentistry) in combination with Edelweiss nanohybrid resin composite (Edelweiss Dentistry) and Prime\&Bond Universal (Dentsply Sirona) adhesive system. In Group 2; 36 teeth (11 patients) were restored with Ceram-X Duo SphereTec (Dentsply Sirona) resin composite in combination with U- veneer (Ultradent) transparent templates and Prime\&Bond Universal adhesive systems. Properties of the restorations were evaluated at baseline, 6, 12, 24, and 36 months using Modified Ryge Criteria (USPHS Criteria). Data were evaluated using Chi-Square and Fisher's Exact tests (p=0.05).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
6-year clinical performance of prefabricated and clear template-formed resin composite veneers.
Bilen H, Turkun LS. · · 2025 · cited 1× · PMID 41125803 · DOI 10.1007/s00784-025-06575-z
Verify or expand the search:
- PubMed search for NCT05984472
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05984472 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Ege University
- Last refreshed: 9 August 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05984472.
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