Template-guided implantation of one-piece ceramic implants. A prospective clinical pilot study.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00012927

Enrollment

Registered

2017-09-07

Start date

2017-09-18

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

K08.1

Interventions

Group 1: Template-guided implantation of one-piece full-ceramic implants with a new, sleeveless drilling template.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Gaps in the upper and / or lower jaw tooth area Free-ending situations in the upper and / or lower jaw area The extraction is at least 3 months. Only early implantations (3 - 6 months post-extraction) and late implantation (> 6 months post-extraction) are performed. The template must be applied to the tooth. For this purpose, more than 5 residual teeth must be present in the jaw to be implanted. The patient has good oral hygiene and compliance. A preimplantological hygiene phase must be completed. Patient's consent.

Exclusion criteria

Exclusion criteria: Persons under 18 or not legally competent persons Untreated acute periodontitis with pocket depths> 4 mm. Strong smokers (more than 10 zig / d) Taking bisphosphonates Pregnant Alcohol or drug addicts Patients with an infectious disease such as hepatitis or HIV or AIDS Patients with severe diabetes m. immediate implantation Width of the gap in the mesio-distal direction with single tooth gaps> 7.1 mm.

Design outcomes

Primary

Measure	Time frame
Deviation of the planned implant position from the actual position. The deviation is described by the distance at the crestal implant penetration point, at the apical end of the implant, at the height of the implant and in the axis deviation. The measurement will be performed immediately after insertion of the implant.	—

Secondary

Measure	Time frame
Indication limitations for the stencil design of 2ingis. Clinical complications: Insufficient template content, eg. Technical complication: stencil fracture or the like. Feasibility study for a subsequent multicentric field study. The feasibility study should give evidence of a sufficient clinical accuracy of the used templates and work out possible indication restrictions. All recordings are made on the day of Implantation. No further follow-up is performed.	—

Measure

Time frame

Indication limitations for the stencil design of 2ingis. Clinical complications: Insufficient template content, eg. Technical complication: stencil fracture or the like. Feasibility study for a subsequent multicentric field study. The feasibility study should give evidence of a sufficient clinical accuracy of the used templates and work out possible indication restrictions. All recordings are made on the day of Implantation. No further follow-up is performed.

—

Countries

Germany

Contacts

Public ContactSigmar Schnutenhaus

Private Praxis und Universitätsklinikum Ulm, Klinik für Zahnärztliche Prothetik

sigmar.schnutenhaus@uniklinik-ulm.de07731 182755

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026