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Immediate Loading of Implants in the Partially or Completely Edentulous Jaw

Immediate Loading of Implants in the Partially or Completely Edentulous Jaw

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02661412
Acronym
IMLOAD
Enrollment
150
Registered
2016-01-22
Start date
2015-12-31
Completion date
2031-12-31
Last updated
2022-02-28

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

Conditions

Jaw, Edentulous, Jaw, Edentulous, Partially

Keywords

immediate loading, biological stability, mechanical stability, long-term, marginal bone level, maxilla, immediate placement, dental implant, fibre-reinforced provisional fixed prosthesis

Brief summary

The investigators aim to evaluate the biological and mechanical short- and long-term outcome of IL in partially or completely edentulous patients. Moreover, the investigators aim to detect potential influencing risk factors predicting undesirable prosthetic outcome.

Detailed description

Since its introduction in the late 1990s, immediate implant loading concepts (IL) have become a frequent alternative for delayed implant procedures. IL concepts reduce chair time, the number of surgical interventions and pain, and offer instant comfort to the patient. Its reduced treatment time results in obvious socioeconomic advantages. Although there is at present abundant evidence that supports IL, evaluation of long-term biological and mechanical stability outcomes of large patient populations could allow quality improvement and more accurate patient selection. The Departments of Oral and Maxillofacial Surgery and the Department of Dentistry of the General Hospital Saint-John Bruges act as one of the pioneers of IL in Belgium, routinely performing the concept since 2001. The investigators aim to evaluate the biological and mechanical short- and long-term outcome of IL in partially or completely edentulous patients. Moreover, the investigators aim to detect potential influencing risk factors predicting undesirable prosthetic outcome.

Interventions

None listed

Sponsors

AZ Sint-Jan AV
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients of all ages * patients of all genders * patients with partially or complete edentulous jaw * patients treated at the department between 01/01/2001 and 31/12/2015

Exclusion criteria

* patients not eligible according to abovementioned criteria * patients who required horizontal bone augmentation procedures of the complete alveolar bone * patients who required a jaw reconstruction after tumor resection, osteoradionecrosis or medication-related osteonecrosis of the jaw

Design outcomes

Primary

MeasureTime frameDescription
implant survival ratewithin 6 months post placement of implantsPercentage of people in the study for which implant is still present of the fixture in the oral cavity

Secondary

MeasureTime frameDescription
Infection ratewithin 6 months post placement of implantsPercentage of people in the study that develop an infection at the site of the implant in the oral cavity
correlation between patient-mediated factors and occurrence of implant instabilitywithin 6 months post placement of implantscorrelation between patient-mediated factors (age, gender, comorbidities, etc) and occurrence of implant instability, as clinically evaluated by the treating surgeon
correlation between clinical factors and the occurrence of implant instabilitywithin 6 months post placement of implantscorrelation between clinical factors (surgeon, surgical procedure, etc) as and the occurrence of implant instability, as clinically evaluated by the treating surgeon
correlation between implant characteristics and occurrence of implant instabilitywithin 6 months post placement of implantscorrelation between implant characteristics (design/finish/material) and occurrence of implant instability, as clinically evaluated by the treating surgeon

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026