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COMPLETED NA

Study Comparing Appearance and Function of Three Different Dental Implant Designs When Placed in Front Region of Upper Jaw

NCT00820235 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective is to compare the gum response to three different dental implant designs when placed in the front region of the upper jaw. The changes from baseline to one year after will be compared. The null-hypothesis is that the buccal soft tissue (gum) changes from baseline to one year after are equal for all three implant-abutment interface settings.

Conditions Studied

Interventions

  • DEVICE OsseoSpeed™
  • DEVICE NobelSpeedy™ Replace®
  • DEVICE NanoTite™ Certain® PREVAIL®

Study Locations (4)

Iowa

  • University of Iowa, College of Dentistry — Iowa City

North Carolina

  • University of North Carolina, School of Dentistry — Chapel Hill

Texas

  • Perio Health Clinical Research Center — Houston

Quebec

  • Faculty of Dentistry, McGill University — Montreal

Trial Details

FieldValue
Enrollment Target 141 participants
Start Date 2009-02
Est. Completion 2016-09
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00820235

The ClinicalTrials.gov registry entry for NCT00820235 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 141 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dentsply Sirona Implants and Consumables, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Jaw, Edentulous, Partially appearing as the primary indexed condition, and to 3 interventions — of which OsseoSpeed™ is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00820235 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Iowa, North Carolina, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00820235 about?

NCT00820235 is a clinical study titled "Study Comparing Appearance and Function of Three Different Dental Implant Designs When Placed in Front Region of Upper Jaw". The primary objective is to compare the gum response to three different dental implant designs when placed in the front region of the upper jaw. The changes from baseline to one year after will be compared. The null-hypothesis is that the buccal soft tissue (gum) changes from baseline to one year af...

What is the current status of trial NCT00820235?

This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2009-02. Estimated completion is 2016-09.

What conditions does trial NCT00820235 study?

This clinical trial studies the following conditions: Jaw, Edentulous, Partially. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00820235?

The interventions under investigation include: OsseoSpeed™ (DEVICE), NobelSpeedy™ Replace® (DEVICE), NanoTite™ Certain® PREVAIL® (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00820235?

This trial is sponsored by Dentsply Sirona Implants and Consumables, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00820235 being conducted?

This trial has 4 study locations across Iowa, North Carolina, Texas, Quebec. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial