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

Completed

Conditions: Tandwortel implantaten
Dental implants

Registration Number: NL-OMON35693

Lead Sponsor: Vrije Universiteit Medisch Centrum

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 27

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

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

Study & Design

Study Type: Observational non invasive

Study Design: Not specified

Primary Outcome Measures

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

Secondary Outcome Measures