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Clinical validation of a digital CAD/CAM technology-based Surgical Guide system with limited intermaxillary space overcoming technology

Clinical validation of a digital CAD/CAM technology-based Surgical Guide system with limited intermaxillary space overcoming technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011096
Enrollment
57
Registered
2025-11-05
Start date
2024-08-07
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

None listed

Interventions

None listed

Sponsors

Osstem Implant
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with loss of one or two second premolars or molars, making them eligible for implant placement. Implant fixtures to be placed have a diameter of 4.0 mm or greater and a length of 7.0 mm or greater. Participants who have agreed to participate in this study and have provided written informed consent.

Exclusion criteria

Exclusion criteria: Patients with restricted mouth opening (trismus) that precludes intraoral scanning and guided implant surgery. Patients requiring extensive bone grafting procedures. Patients exhibiting a tooth mobility of Grade II or greater in the teeth serving as support for the surgical guide.

Design outcomes

Primary

MeasureTime frame
Evaluation of implant placement accuracy through analysis of horizontal, vertical, and angular deviations.

Secondary

MeasureTime frame
Variables for safety assessment: fit precision, presence of fractures, and postoperative abnormalities

Countries

Korea, Republic of

Contacts

Public ContactSu Young Lee

The Catholic University of Korea, Seoul St. Mary's Hospital

lsuyoung@daum.net+82-2-2258-1795

Outcome results

None listed

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