Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00607022 · ClinicalTrials.gov registry record · NA
A Randomized Prospective Clinical Trial Comparing Single Tooth Implant 3 Loading Protocols
A NA study of Dental Implant, sponsored by Clark Stanford.
- Completed
- Registry status
- NA
- Development phase
- 41
- Enrollment target
- 1
- Study location
NCT00607022: Completed NA study of Dental Implant, sponsored by Clark Stanford.
NCT00607022 is a NA study of Dental Implant that has completed, run by Clark Stanford. The registered enrollment target is 41 participants, above the 30-participant average among 8 other Dental Implant trials with a reported enrollment target (37% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00607022, a NA study of Dental Implant, has completed, sponsored by Clark Stanford.
- COMPLETED
- Registry status
- NA
- Development phase
- 41 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Primary Outcome
The objective of this study is to examine the change in implant stability upon three different loading regimens during the first sixteen weeks following implant placement. ISQ score (1-100), where higher score equals more stability, was assessed. The main hypotheses of the study are 1) Implant stability (ISQ) is minimally affected when physiologic load is applied to an implant during the healing process.
Conditions Studied
Interventions
- DEVICE dental implant
Study Locations (1)
Iowa
- The University of Iowa College of Dentistry - Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2007-12 |
| Est. Completion | 2013-06 |
| Phase | NA |
What the finished NCT00607022 record still lists
NCT00607022 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, above the 30-participant average among 8 other Dental Implant trials with a reported enrollment target (37% higher).
The record links to 1 condition, with Dental Implant appearing as the primary indexed condition, and to 1 intervention - of which dental implant is the first listed.
NCT00607022 reports a single indexed study location in Iowa.
Frequently Asked Questions
What is clinical trial NCT00607022 about?
NCT00607022 is a clinical study titled "A Randomized Prospective Clinical Trial Comparing Single Tooth Implant 3 Loading Protocols". 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...
What is the current status of trial NCT00607022?
This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2007-12. Estimated completion is 2013-06.
What conditions does trial NCT00607022 study?
This clinical trial studies the following conditions: Dental Implant.
What interventions are being tested in trial NCT00607022?
The interventions under investigation include: dental implant (DEVICE).
Who is sponsoring clinical trial NCT00607022?
This trial is sponsored by Clark Stanford, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00607022 being conducted?
This trial has 1 study location across Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Dental Implant
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00607022's enrollment target sits among peer trials
41 3rd of 8 higher than 5 of 8 other Dental Implant trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Dental Implant trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Ridge Augmentation Using Allograft Particles Hydrated With or Without Recombinant Human Platelet-Derived Growth Factor
RECRUITING · NA
-
Closed Sinus Augmentation With a Calcium Phosphosilicate Putty
RECRUITING · NA
-
Evaluation of Sinus Augmentation Bone Healing Using Autograft and Xenograft Compared to Xenograft Alone
ACTIVE NOT RECRUITING · NA
-
Longitudinal Study of Dental Implant Therapy in HIV Positive Patients
COMPLETED · NA
-
Evaluation of Zimmer Puros® Allograft vs. Creos™ Allograft for Alveolar Ridge Preservation
COMPLETED · NA
-
To Compare Different Soft Tissue Grafts at the Time of Lateral Ridge Augmentation Procedure.
COMPLETED · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03449238 · 41 participants · Phase 1
Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients
- NCT03900793 · 41 participants · Phase 1
Losartan + Sunitinib in Treatment of Osteosarcoma
- NCT04082520 · 41 participants · Phase 2
Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy
- NCT04220190 · 41 participants · Phase 2
RAPA-501 Therapy for ALS
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia