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Accuracy of dental implant positioning by dynamic or static computer-assisted implant surgery: a randomized controlled clinical trial

Accuracy of dental implant positioning by dynamic or static computer-assisted implant surgery: a randomized controlled clinical trial - RCT Dynamic Navigation Implants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00038401
Enrollment
70
Registered
2025-11-18
Start date
2019-08-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Missing tooth, which shall be replaced by an implant with prosthetic restoration.

Interventions

Group 1: - The indication was the absence of a tooth that was to be replaced with a dental implant. - In 35 cases, the implant position was digitally planned based on a 3D diagnostics by CBCT dataset

Sponsors

Poliklinik für Zahnerhaltung, Parodontologie und digitale Zahnmedizin, Klinikum der Universität München, LMU München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criterion was the indication for the insertion of at least one dental implant. Only patients for whom a Cone Beam Computed Tomography (CBCT) scan was indicated based on the S2k guidelines on indications for 3D radiographic diagnostics and computer-assisted implantology (DGZMK 2012, 2022) were included.

Exclusion criteria

Exclusion criteria: Exclusion criteria included minors and individuals with disabilities for whom legally valid informed consent could not be obtained. In addition, the following absolute/relative contraindications to implant placement should be observed (even though they are not specific to the study per se; Maas, 2011). These are consistent with the S2k guideline on indications for 3D diagnostics and computer-assisted implantology (DGZMK 2012, 2022), including: Children and adolescents Severe cardiovascular disease Severe coagulation disorders (coagulopathies) Autoimmune diseases / immunodeficiencies Immunosuppression after transplantation Significant metabolic disease Poorly controlled diabetes mellitus High-dose systemic corticosteroid therapy History of radiotherapy/chemotherapy Bone diseases Bone tumors Paget’s disease of bone Current or prior bisphosphonate or denosumab therapy (medications associated with medication-related osteonecrosis of the jaw, MRONJ) Substance or alcohol abuse Heavy smoking (nicotine abuse) Lack of compliance / poor adherence

Design outcomes

Primary

MeasureTime frame
Primary outcomes: - 3D angular deviation of the implant axis (°), - 3D deviation of the implant base, and tip (mm). Time of measurement: - 3 months after implant placement, i.e. after healing Method of data acquisition: - Matching of 3D implant planning data, and actual clinical position of implant (3D scan of scan body fixed on implant)

Secondary

MeasureTime frame
- 2D mesio-distal deviation of the implant base, and tip (mm); - 2D vestibulo-oral deviation of the implant base, and tip (mm); - 2D apico-coronal deviation of the implant base, and tip (mm) (deviation in depth).

Countries

Czechia

Contacts

Public ContactKarin Christine Huth

Poliklinik für Zahnerhaltung, Parodontologie und digitale Zahnmedizin, Klinikum der Universität München, LMU München

karin.huth@med.uni-muenchen.de+4989440059301

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026