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Chronological changes in the stability and marginal bone level of immediately loaded NobelActive implants using NobelGuide for edentulous maxilla: one-year prospective clinical study

Chronological changes in the stability and marginal bone level of immediately loaded NobelActive implants using NobelGuide for edentulous maxilla: one-year prospective clinical study - Chronological changes in the stability and marginal bone level of immediately loaded Implants for edentulous maxilla

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007637
Enrollment
40
Registered
2012-04-01
Start date
2011-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Edentulous maxilla

Interventions

Placement of NobelActive implants using NobelGuide for edentulous maxilla and application of immediate Load

Sponsors

Section of Implant and Rehabilitative Dentistry, Division of Oral Rehabilitation, Kyushu University Faculty of Dental Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients older than 20 years agreed to participate in this study 2) Edentulous maxilla(More than three months After extraction) 3) Four or more implants can be inserted into the maxilla

Exclusion criteria

Exclusion criteria: 1) Systemic disease that would interfere with dental implant therapy (e.g.uncontrolled diabetes) 2) Any contraindications for oral surgical procedures 1.Are taking medications that interfere with treatment (Bisphosphonate drugs ,Steroid , Anticoagulant etc.) 2.Leukocyte dysfunction or deficiency 3.Unmanageable bleeding disorders 4.Neoplastic disease that require Radiotherapy and Chemotherapy 5.Immunodeficiency and Immunological deterioration 6.Patients with metabolic bone disease 7.Poor oral hygiene , Physical or mental handicaps that would interfere with the ability to perform adequate oral hygiene 8.Severe periodontitis 9.Mucosal diseases (e.g. erosive lichen planus and Erosive leukoplakia) 10.History of local irradiation therapy in the head / neck area 11.Drug dependence and Alcoholism 12.Dysfunction of wound healing 13.Patients who have not completed bone growth 14.Xerostomia 15.Titanium allergy 16.Unmanageable Endocrine disease 3)Subjects who have undergone administration of any investigational device within 30 days of enrolment in the study 4)Pregnant or breastfeeding women 5) Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance or unreliability 6)Bone augmentation has been applied for the implant insertion site

Design outcomes

Primary

MeasureTime frame
1.Chronological change of implant stability 2.Chronological change of marginal bone level 3.Factors affecting stability and marginal bone level 4. Evaluation of patient satisfaction

Secondary

MeasureTime frame
1. Chronological change of occlusal force 2.Correlation between marginal bone level and PPD,BOP,PI 3. Relationship between insertion torque and ISQ

Countries

Japan

Contacts

Public ContactJunichi Yamada

Fukuoka Tenjin Implant Clinic Fukuoka Tenjin Implant Clinic

ymd1966@dent.kyushu-u.ac.jp092-738-4618

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026