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NCT05355792
Multicenter Study to Evaluate the Clinical Outcome of the OmniTaper EV Implant in Single Tooth Restorations
NA trial testing OmniTaper EV implants in Jaw, Edentulous in 139 participants. Participants enrolled and being followed up; not accepting new ones.
30 November 2028
Quick facts
| Lead sponsor | Dentsply Sirona Implants and Consumables |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 139 |
| Start date | 22 September 2022 |
| Primary completion | 30 November 2028 |
| Estimated completion | 31 January 2029 |
| Sites | 6 locations across United Kingdom, Switzerland, Germany |
Drugs / interventions tested
- OmniTaper EV implants
Conditions studied
- Jaw, Edentulous — all drugs for Jaw, Edentulous →
Sponsor
Dentsply Sirona Implants and Consumables — full company profile →
Who can join
Adults 18 to 75, any sex, with Jaw, Edentulous. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This clinical study, funded by the company Dentsply Sirona, is being carried out to see if the newly developed tooth implant "OmniTaper EV" is safe, effective and functions as intended when replacing a lost or removed tooth. The OmniTaper EV implant is a further development of existing dental implants. It is made of titanium, a metal that is well tolerated by the human body, which has been successfully used in dental implants for more than 40 years. All components used in this study are available on the market, are CE-marked and will be used according to intended use and approved instructions. The study involves at 11 planned clinic visits including follow-up visits 6 months and annually until 5 years after installation of the permanent crown. after over a period of about five and a half years. The treatment method and healing period may vary depending on the individual case and treatment plan and additional visits may therefore need to be scheduled. The visits and procedures are the same as standard of care and no procedures will be done just for purpose of research. The study aims to recruit about 137 men and women from six clinics across Europe (Germany, UK and Switzerland) and participants can only receive one study implant each. Participation is entirely voluntary and participants can choose to withdraw from the study at any time, without giving a reason. The decision to decline or withdraw participation will not affect participants future treatment or care
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05355792
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
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Related trials
Other Dentsply Sirona Implants and Consumables trials
Trials by the same sponsor.
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- NCT06539676 — A Study to Compare Nighttime Aligners to Daytime Aligners · NA · terminated
- NCT05752539 — Clinical Evaluation of Implants Restored With Advanced Lithium Disilicate Screw-retained Crowns · active not recruiting
- NCT05751382 — Evaluation of Self-adhesive Hybrid Resin Composite Compared to a Traditional Composite Resin in Restorations of NCCLs · NA · terminated
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 NCT05355792 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Dentsply Sirona Implants and Consumables
- Last refreshed: 17 February 2026
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/NCT05355792.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing