A randomized controlled clinical trial to compare the immediate and delayed loading implant protocol evaluating clinical aspects.

A randomized controlled clinical trial to compare the immediate and delayed loading implant protocol evaluating clinical aspects. - compare the immediate and delayed loading implant protocol

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON35693

Enrollment

Registered

2010-12-13

Start date

2012-05-25

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

Tandwortel implantaten Dental implants

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age between 20-80 Missing (pre) molar in the right and left quadrant of the jaw Patients will be seen for a strict hygiene protocol every three months

Exclusion criteria

Exclusion criteria: Exclusion criteria: Physical and mental disabilities which interfere with the maintenance of implants Severe skeletal jaw discrepancies. Severe clenching habits Those that have already received or lost implants Patients with periodontitis Drugs or alcohol abuse. Having received radiotherapy to the head and neck region for malignancies Heavy smokers (more than a 10 cigarettes a day) Undergoing chemotherapy On long-term therapy with steroids, immunosuppressants or biphosphates Insulin-dependent diabetic patients and uncontrolled onset diabetic patients Those affected by chronic renal or liver disease Systemic and local bone disorders and pathology Serious cardiac and pulmonary disorders Hemophiliac disorders who are susceptible for increase bleeding and tendency for post-operative infections Those who are at risk of developing bacterial endocarditis, (cardiac valve disease, prosthetic valves or previous episodes of bacterial endocarditis) Immuno-compromised patients, including those with HIV

Design outcomes

Primary

Measure	Time frame
Clinical parameters: Periodontal parameters will be documented in a standardized method evaluating the scenario of the treatment at implant insertion, after inserting the final restoration after 6 months, 12 months and then after 2 years. These are the plaque and bleeding index according to Mombelli et al, the marginal bone height and the probing depth. These are all measured at the buccal, distal, lingual and mesial position around the implants. Radiographs A digital periapical radiograph will be taken of each implant at the time of implant placement. The second radiograph is taken at abutment connection (6 weeks). The following X-ray evaluation is at 6 months, 12 months and 2 years.	—

Measure

Time frame

Clinical parameters: Periodontal parameters will be documented in a standardized method evaluating the scenario of the treatment at implant insertion, after inserting the final restoration after 6 months, 12 months and then after 2 years. These are the plaque and bleeding index according to Mombelli et al, the marginal bone height and the probing depth. These are all measured at the buccal, distal, lingual and mesial position around the implants. Radiographs A digital periapical radiograph will be taken of each implant at the time of implant placement. The second radiograph is taken at abutment connection (6 weeks). The following X-ray evaluation is at 6 months, 12 months and 2 years.

—

Secondary

Measure	Time frame
3% loss implants lower jaw 5% loss implants upper jaw	—

Countries

Netherlands

Outcome results