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Clinical evaluation of kS? BA Extra-short dental implants in posterior maxilla

Clinical evaluation of kS? BA Extra-short dental implants in posterior maxilla

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009845
Enrollment
18
Registered
2024-10-14
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-03

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 : Placing two kSIII BA Ø5.0 x 3.0 mm implants without sinus lift in the maxillary posterior edentulous area.

Sponsors

Seoul National University Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults aged between 19 and 75 years who are scheduled for implant placement in the maxillary posterior edentulous area at Seoul National University Dental Hospital and have provided written consent. Patients with a residual alveolar bone width of at least 7 mm and a vertical distance of 3-5 mm from the residual alveolar bone to the maxillary sinus. Individuals with at least 20 remaining teeth, including any artificial teeth in the oral cavity. Patients with a plaque index and bleeding on probing index of less than 20%. Patients who have received a detailed explanation of the study, understood it, and have voluntarily decided to participate and provided consent.

Exclusion criteria

Exclusion criteria: Individuals with systemic diseases that could affect treatment outcomes. Patients who have experienced unstable angina, myocardial infarction, or transient ischemic attack within the last six months. Individuals who have undergone coronary angioplasty (PTCA) or coronary artery bypass grafting (CABG). Patients who have experienced severe cerebrovascular accidents (stroke, cerebral infarction, cerebral hemorrhage, etc.) within the last six months. Those with clinically significant renal or liver function abnormalities. Patients with uncontrolled diabetes. Individuals deemed unsuitable for participation in this study by the principal investigator or attending staff.

Design outcomes

Primary

MeasureTime frame
Implant stability

Secondary

MeasureTime frame
Implant survival rate

Countries

Korea, Republic of

Contacts

Public ContactSUN HEE PARK

Seoul National University Dental Hospital

p101911@naver.com+82-2-6256-3144

Outcome results

None listed

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