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Randomized, prospective clinical investigation regarding the accuracy of transferred implant position and the influence of the prosthetic materials used with a view to surrounding hard and soft tissues

Randomized, prospective clinical investigation regarding the accuracy of transferred implant position and the influence of the prosthetic materials used with a view to surrounding hard and soft tissues - CSI 2.0

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00033852
Enrollment
80
Registered
2024-03-08
Start date
2024-04-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Loss of teeth K08

Interventions

Group 1: Replacement of a missing tooth with an dental implant. The aim of this study is to compare the accuracy of the planned and transferred implant position and to investigate the influence of the

Sponsors

Charité - Universitätsmedizin Berlin, Abteilung für Zahnärztliche Prothetik, Alterszahnmedizin und Funktionslehre
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - tooth-limited (single-tooth) gaps and free-end situations/shortened dental arches - the patient has been informed about the scheduled follow-up examinations and agrees to attend them

Exclusion criteria

Exclusion criteria: - systemic diseases that preclude implant surgery (e.g. uncontrolled diabetes) - all contraindications for oral surgery - Chemotherapy or radiotherapy in the head and neck area - chronic inflammation (e.g. rheumatoid arthritis) - systemic diseases and metabolic disorders that are associated with bone lesions or bone healing - the use of medication that influences or disrupts bone remodelling (e.g. bisphosphonates) - intraoral infections - patients who are unable to perform adequate oral hygiene - factors which, in the opinion of the examiner, prevent completion of the examination, e.g. unreliability

Design outcomes

Primary

MeasureTime frame
Deviation of the planned implant position from the transferred implant position (crestal).

Secondary

MeasureTime frame
Deviation of the planned implant position from the transferred implant position (apical) and examination of changes in marginal bone levels, soft tissues, esthetics, occlusion and patient satisfaction before the beginning of the study and at 3, 12, 24, 36, 48, 60 months after loading of respective implants.

Countries

Germany

Contacts

Public ContactMagdalena Bennett

Charité - Universitätsmedizin Berlin, Abteilung für Zahnärztliche Prothetik, Alterszahnmedizin und Funktionslehre

magdalena.bennett@charite.de+49 30 450 562 712

Outcome results

None listed

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