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Single-blind confirmatory, prospective, and single-organization clinical trial to obtain safety and effectiveness of dental implants according to implantation type

Single-blind confirmatory, prospective, and single-organization clinical trial to obtain safety and effectiveness of dental implants according to implantation type

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006116
Enrollment
66
Registered
2021-05-04
Start date
2021-05-18
Completion date
Unknown
Last updated
2022-11-28

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 : 1. gum level: No extra surgery by treating implants to show above the tissue. - control: Straumann SLA tissue level - experimental: Neobiotech IT-III Active 2. Bone level: Place impl

Sponsors

NeoBiotech
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? A person who has completed the growth of the bones between 19 and 75 years of age. ? Patients with premolars or molars defects on either side of the mandible ? Those who do not have severe incongruity between maxillary and mandibular relationships ? Those with sufficient vertical, buccal, and mesial-centered available bones ? A person who is sure of the patient motivation for implant treatment ? A person who agrees to participate in a clinical trial and signs a subject's consent form.

Exclusion criteria

Exclusion criteria: ? Pregnant women and the elderly and the weak who are unable to recover and operate ? A person with a history of cerebral infarction, cerebral hemorrhage, angina, and myocardial infarction ? A person who has an uncontrolled internal disease ? A person with an uncontrolled hemorrhagic disease ? A person suspected of mental illness or has a mental illness ? Those who have hypersensitivity to the implant material ? Those who have received radiation therapy, chemotherapy, or bone resorption inhibitory treatment ? Others who are inappropriate to participate in clinical trials as judged by the person in charge of clinical trials as they may affect the results of clinical trials ethically

Design outcomes

Primary

MeasureTime frame
Survival rate(%)

Secondary

MeasureTime frame
Implant stability quotient;Alveolar bone loss;Difference in survival rate between tissue level and bone level (%);Periodontal examination (Furcation, Bleeding on Probing, Probing Depth);Implant stabillity test

Countries

Korea, Republic of

Contacts

Public ContactJeongmin Ko

Korea University Anam Hospital

als8237@korea.ac.kr+82-2-920-5358

Outcome results

None listed

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