A Randomized Prospective Clinical Trial Comparing Single Tooth Implant 3 Loading Protocols
| Status: | Completed |
|---|---|
| Conditions: | Dental |
| Therapuetic Areas: | Dental / Maxillofacial Surgery |
| Healthy: | No |
| Age Range: | 18 - 80 |
| Updated: | 7/29/2018 |
| Start Date: | December 2007 |
| End Date: | June 2013 |
the Effects of 3 Loading Protocols on Dental Implant Stability in Healed Ridges
This is a research study to test the clinical procedure and not the FDA approved medical
device. This project will screen up to 80 volunteers to enroll 40 active subjects to receive
a single tooth implant on an anterior (incisor/canine) or pre-molar tooth in the mandible or
maxilla (no implants will be placed in molar sites). This 3 year research study will examine
the clinical effects of loading regimens on roughened surfaced implants. The proposed
research project will measure the changes in mucosal healing and maturation over a three year
period following implant placement. The proposed research lays the foundation for improved
health care by providing surgeons and restorative dentists with data for determining the
relationship between implant healing, loading pattern and bone type. The rationale that
underlies the investigation is that identification of the influences of timing of load on
implant stability in varying bone types will allow routine, predictable use of early loading,
which, in turn, will translate into more rapid health care, and improved psychosocial
well-being of the patient. If these hypotheses are correct, these results are expected to
provide evidence based research data to support early loading and immediate loading of single
implants in sites of adequate bone volume, and density. In addition, it is expected that
these results will fundamentally advance the field of implant dentistry and bioengineering by
providing information on the principles of the bone density-mechanical environment-implant
stability interaction.
device. This project will screen up to 80 volunteers to enroll 40 active subjects to receive
a single tooth implant on an anterior (incisor/canine) or pre-molar tooth in the mandible or
maxilla (no implants will be placed in molar sites). This 3 year research study will examine
the clinical effects of loading regimens on roughened surfaced implants. The proposed
research project will measure the changes in mucosal healing and maturation over a three year
period following implant placement. The proposed research lays the foundation for improved
health care by providing surgeons and restorative dentists with data for determining the
relationship between implant healing, loading pattern and bone type. The rationale that
underlies the investigation is that identification of the influences of timing of load on
implant stability in varying bone types will allow routine, predictable use of early loading,
which, in turn, will translate into more rapid health care, and improved psychosocial
well-being of the patient. If these hypotheses are correct, these results are expected to
provide evidence based research data to support early loading and immediate loading of single
implants in sites of adequate bone volume, and density. In addition, it is expected that
these results will fundamentally advance the field of implant dentistry and bioengineering by
providing information on the principles of the bone density-mechanical environment-implant
stability interaction.
MATERIALS AND METHODS This longitudinal human clinical trial is designed as a prospective
study, to measure implant stability with the resonance frequency analyzer (Osstell,
Integration Diagnostics AB, Sweden) at time of implant placement and up to 16 weeks post
placement. After 16 weeks, a definitive implant abutment will be placed and a final dental
crown delivered. No further follow-up will be done with the resonance frequency approach.
However, all subjects will be followed through 3 years post implant placement as described
for each follow-up visit. The study population consists of subjects at the University of
Iowa's College of Dentistry. Subjects presenting with one tooth missing in the anterior
(incisor/canine) or pre-molar regions of the mandible or maxilla with existing teeth that
were healthy or adequately restored shall be screened based on the inclusion/exclusion
criteria. The missing tooth is to be replaced with a fixed implant restoration on one
implant.
SEQUENCE OF VISITS A. Visit 1: Screening Examination
Subjects shall be seen for evaluation and for collection of baseline data. Pre-treatment data
shall be recorded on case report forms. The visit shall include:
1. Explanation to the patient of the purposes of the study and the planned procedures
related to the study.
2. Explanation to the subject of the risks and possible complications of participation in
the study. Patients shall be notified that inclusion in the study is for the purpose of
providing implant treatment only and that no provision for other active treatments are
guaranteed or implied except for care related to the implant aspect of their oral
cavity. This treatment shall be agreed upon as outlined for their specific case.
Implant Site Selection: Adequate bone volume is needed to accommodate the planned endosseous
dental implant. This will mean sufficient height such that the implant would not encroach on
vital structures (such as inferior alveolar nerve), and sufficient width that the implant
could be placed within the confines of the existing bone without dehiscence or fenestration,
requiring significant grafting at time of implant placement. Typically, this will mean space
dimensions will be: 6 mm or greater ridge width facial-lingual and > 6 mm in the mesial to
distal dimension . If the implant can be placed and only a few screw threads are exposed,
grafting is allowed to cover these threads. In the planned occlusal-gingival dimension, there
must be at least 7 mm of space from the planned head of the implant to the planned occlusal
plane.
The subject should be notified that inclusion in the study is conditional upon satisfying the
inclusion and exclusion criteria as seen in Table 1. Only subjects satisfying the
Inclusion/Exclusion criteria shall be enrolled.
The dental implant system to be used is the Astra Tech OsseoSpeed Dental Implant System
(Astra Tech AB, Mölndal Sweden). This is an FDA cleared product under FDA 510k clearance act
(FDA clearance 4/30/2004). This protocol calls for use of only the 4.0 mm diameter by 11 mm
long dental implant (OsseoSpeed Aqua platform; Ref Number 24622; Astra Tech AB) in the
anterior (incisor/canine) or posterior pre-molar regions of the mandible or maxilla. All
sites must have sound natural or restored teeth/implants Mesial and Distal to the planned
site of interest (Bounded Edentulous Space or BES). The patient should otherwise have a
restored stable occlusion that is mutually protected. No implants will be placed in molar
sites. The implant lengths accepted in the study are 11 mm. Clinical and radiographic
screening will be used to limit the study to patients with sufficient bone quantity to
completely encase the implant.
Upon review of the subject's health history, inclusion/exclusion criteria a screening
clinical assessment will be made. Existing dental radiographs within the past 6 months shall
be acceptable. No new radiographs will be made until subject enrollment and obtaining signed
informed consent. The subject will be given an informed consent for the study and reviewed
with the clinical study coordinator. Preliminary diagnostic impressions will made (Penta, 3M
ESPE) and poured in dental stone (Whip Mix Corp., Louisville, KY). Implant subjects may have
a pre-operative Cone Bean CT imaging study (Galileos; Sirona, Charlotte NC; www.sirona.com)
made at the College of Dentistry's Department of Oral Maxillofacial Radiology at the
discretion of the Principal Investigator following diagnostic work-up. Subjects shall be
either patients of record of the College of Dentistry or shall be enrolled if new to the
College. Patient records are electronic (WinDent) along with a paper version. Paper-based
Case Report Forms (CRF) containing subject's medical information will be kept in one central
file in a locked cabinet in the Dental Clinical Research Center. This data will be kept in a
secured file accessible only by the PI and the Clinical Coordinator.
study, to measure implant stability with the resonance frequency analyzer (Osstell,
Integration Diagnostics AB, Sweden) at time of implant placement and up to 16 weeks post
placement. After 16 weeks, a definitive implant abutment will be placed and a final dental
crown delivered. No further follow-up will be done with the resonance frequency approach.
However, all subjects will be followed through 3 years post implant placement as described
for each follow-up visit. The study population consists of subjects at the University of
Iowa's College of Dentistry. Subjects presenting with one tooth missing in the anterior
(incisor/canine) or pre-molar regions of the mandible or maxilla with existing teeth that
were healthy or adequately restored shall be screened based on the inclusion/exclusion
criteria. The missing tooth is to be replaced with a fixed implant restoration on one
implant.
SEQUENCE OF VISITS A. Visit 1: Screening Examination
Subjects shall be seen for evaluation and for collection of baseline data. Pre-treatment data
shall be recorded on case report forms. The visit shall include:
1. Explanation to the patient of the purposes of the study and the planned procedures
related to the study.
2. Explanation to the subject of the risks and possible complications of participation in
the study. Patients shall be notified that inclusion in the study is for the purpose of
providing implant treatment only and that no provision for other active treatments are
guaranteed or implied except for care related to the implant aspect of their oral
cavity. This treatment shall be agreed upon as outlined for their specific case.
Implant Site Selection: Adequate bone volume is needed to accommodate the planned endosseous
dental implant. This will mean sufficient height such that the implant would not encroach on
vital structures (such as inferior alveolar nerve), and sufficient width that the implant
could be placed within the confines of the existing bone without dehiscence or fenestration,
requiring significant grafting at time of implant placement. Typically, this will mean space
dimensions will be: 6 mm or greater ridge width facial-lingual and > 6 mm in the mesial to
distal dimension . If the implant can be placed and only a few screw threads are exposed,
grafting is allowed to cover these threads. In the planned occlusal-gingival dimension, there
must be at least 7 mm of space from the planned head of the implant to the planned occlusal
plane.
The subject should be notified that inclusion in the study is conditional upon satisfying the
inclusion and exclusion criteria as seen in Table 1. Only subjects satisfying the
Inclusion/Exclusion criteria shall be enrolled.
The dental implant system to be used is the Astra Tech OsseoSpeed Dental Implant System
(Astra Tech AB, Mölndal Sweden). This is an FDA cleared product under FDA 510k clearance act
(FDA clearance 4/30/2004). This protocol calls for use of only the 4.0 mm diameter by 11 mm
long dental implant (OsseoSpeed Aqua platform; Ref Number 24622; Astra Tech AB) in the
anterior (incisor/canine) or posterior pre-molar regions of the mandible or maxilla. All
sites must have sound natural or restored teeth/implants Mesial and Distal to the planned
site of interest (Bounded Edentulous Space or BES). The patient should otherwise have a
restored stable occlusion that is mutually protected. No implants will be placed in molar
sites. The implant lengths accepted in the study are 11 mm. Clinical and radiographic
screening will be used to limit the study to patients with sufficient bone quantity to
completely encase the implant.
Upon review of the subject's health history, inclusion/exclusion criteria a screening
clinical assessment will be made. Existing dental radiographs within the past 6 months shall
be acceptable. No new radiographs will be made until subject enrollment and obtaining signed
informed consent. The subject will be given an informed consent for the study and reviewed
with the clinical study coordinator. Preliminary diagnostic impressions will made (Penta, 3M
ESPE) and poured in dental stone (Whip Mix Corp., Louisville, KY). Implant subjects may have
a pre-operative Cone Bean CT imaging study (Galileos; Sirona, Charlotte NC; www.sirona.com)
made at the College of Dentistry's Department of Oral Maxillofacial Radiology at the
discretion of the Principal Investigator following diagnostic work-up. Subjects shall be
either patients of record of the College of Dentistry or shall be enrolled if new to the
College. Patient records are electronic (WinDent) along with a paper version. Paper-based
Case Report Forms (CRF) containing subject's medical information will be kept in one central
file in a locked cabinet in the Dental Clinical Research Center. This data will be kept in a
secured file accessible only by the PI and the Clinical Coordinator.
Inclusion Criteria:
- The patient is 18 years or older.
- Ability to understand and sign the informed consent prior to starting the study.
- Ability and willingness to comply with all study requirements.
- Adequate oral hygiene (defined as an average Modified Sulcus Bleeding Index of 1 or
less and an average Modified Plaque Index of 1 or less).
- Must be a bounded edentulous space.
- Adequate bone volume to accommodate the planned endosseous dental implant (e.g.
sufficient height such that the implant would not encroach on vital structures such as
inferior alveolar nerve, and sufficient width that the implant could be placed within
the confines of the existing bone without dehiscence or fenestration, requiring
significant grafting at time of implant placement). The only implant utilized in this
protocol will be a 4.0 mm diameter by 11 mm long implant (Fixture OsseoSpeed Astra
Tech).
Typically, this will mean space dimensions will be: 6 mm or greater ridge width
facial-lingual and > 6 mm in the mesial to distal dimension . If the implant can be placed
and only a few screw threads are exposed, grafting is allowed to cover these threads. In
the planned occlusal-gingival dimension, there must be at least 7 mm of space from the
planned head of the implant to the planned occlusal plane.
- Osteotome use will be allowed but there must be a minimum of 8mm of bone height from
the alveolar crest to the floor of the sinus. Maximum sinus lift will be 4 mm.
- Existing teeth are healthy and adequately restored, and desired a fixed restoration on
implants.
- Patient has a mutually protected occlusion.
- The patient, if of childbearing potential, had a negative pregnancy test within one
week prior to surgery.
Exclusion Criteria:
- Patients who have smoked cigarettes or chewed tobacco within the past year.
- History of alcoholism or drug abuse within the past 5 years. - Severe bruxing or
clenching habits
- Untreated periodontitis
- Patients at undue risk for an outpatient surgical procedure
- Presence of residual roots at the implant site- Patients with history of site
development (extensive bone augmentation) at the implant site in the past 4 months.
- Placement of implant in an extraction site that had been healing for less than 2
month.
- Presence of local inflammation or mucosal diseases such as lichen planus.
- Uncontrolled diabetes (defined as HA1c > 7.0 percent).
- Current hematologic disorder or chronic use of coumarin (or similar) anti-coagulant
therapies.
- History of leukocyte dysfunction and deficiencies
- Metabolic bone disorders
- History of renal failure
- History of liver disease
- Immunocompromised patients having HIV, RA, SLE or other collagen vascular disorders.
- Chronic corticosteroid use.
- Current chemotherapy
- History of use of IV-based bisphosphonates.
- History of radiation treatment to the head or neck
- Patients requiring grafting of bone or mucosal tissue at the time of implant placement
which would require submersion of the implant during the healing period.
- Use of any investigational drug or device within the 30 day period immediately prior
to implant surgery
- Patients requiring submersion of implants for esthetic reasons.
- Patient requiring ongoing dental treatment in the same quadrant or opposing quadrant
during the initial 16 week healing period.
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