Effectiveness evaluation study of the ChecQ, new product for assessing implant stability

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010117

Enrollment

Registered

2025-01-10

Start date

2025-01-15

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

None listed

Interventions

Medical Device : The study involves a single visit for each participant, targeting patients visiting Seoul National University Dental Hospital for the placement of a superstructure after implant surge

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion Criteria Adults aged 19 years or older. Individuals who have received a detailed explanation of the study, fully understood it, and voluntarily decided to participate with written consent. Individuals willing and able to comply with the study procedures. Implant placement torque of 30 Ncm or higher. Implant fixture diameter of 4.0 mm or 4.5 mm.

Exclusion criteria

Exclusion criteria: Exclusion Criteria Patients with implanted metallic devices such as pacemakers. Patients with uncontrolled diabetes or cardiovascular diseases. Individuals unwilling or unable to provide informed consent for participation. Individuals deemed unsuitable for the study by the principal investigator or study coordinator.

Design outcomes

Primary

Measure	Time frame
Measurement Values by Device	—

Secondary

Measure	Time frame
Resonance Frequency Analysis	—

Countries

Korea, Republic of

Contacts

Public ContactGYEONGSEOK JEONG

Seoul National University Dental Hospital

taekigogo@naver.com+82-2-6256-3144

Outcome results