Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00223405 · ClinicalTrials.gov registry record

Analysis of Enamel Wear Against Ceramic Restorations

A clinical trial of Tooth Wear, sponsored by The University of Texas Health Science Center at San Antonio.

Completed
Registry status
36
Enrollment target
1
Study location

NCT00223405: Completed study of Tooth Wear, sponsored by The University of Texas Health Science Center at San Antonio.

NCT00223405 is a study of Tooth Wear that has completed, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 36 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00223405, a study of Tooth Wear, has completed, sponsored by The University of Texas Health Science Center at San Antonio.

COMPLETED
Registry status
36 participants
Enrollment target
1
Study location

Study Summary

1. To characterize the microstructure (fracture toughness, particle size of ceramic, and inter-particle spacing) of three ceramic materials 2. To test the hypothesis that lower fracture toughness of glass and/or crystal phase in ceramics reduce wear damage of enamel. 3. To test the hypothesis that smaller sized crystals reduce wear damage of enamel. 4. To test the hypothesis that larger inter-particle spacing reduces wear damage of enamel. 5. To test the hypothesis that equivalent wear patterns exist in all directions between enamel versus enamel and ceramic versus enamel. 6. To test the hypothesis that bite force does not correlate with wear rates. 7. To test the hypothesis that salivary flow does not correlate with wear rates. 8. To test the hypothesis that a greater amount of wear is not associated with a loss in vertical dimension of occlusion. 9. To test the hypothesis that a greater amount of wear does not correlate with secondary cementum deposition as part of the passive eruption process. 10. To test the hypothesis that maximum wear occurs early and wear rates level off within the first two years. 11. To test the hypothesis that in vitro wear analysis does not correlate with in vivo wear measurements

Conditions Studied

Interventions

  • DEVICE crown placement

Study Locations (1)

Texas

  • University of Texas Health Science Center at San Antonio - San Antonio

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2003-04
Est. Completion 2009-01

What the finished NCT00223405 record still lists

NCT00223405 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 36 participants, a relatively small participant target.

The record links to 1 condition, with Tooth Wear appearing as the primary indexed condition, and to 1 intervention - of which crown placement is the first listed.

NCT00223405 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT00223405 about?

NCT00223405 is a clinical study titled "Analysis of Enamel Wear Against Ceramic Restorations". 1. To characterize the microstructure (fracture toughness, particle size of ceramic, and inter-particle spacing) of three ceramic materials 2. To test the hypothesis that lower fracture toughness of glass and/or crystal phase in ceramics reduce wear damage of enamel. 3. To test the hypothesis that s...

What is the current status of trial NCT00223405?

This trial is currently completed. The enrollment target is 36 participants. The study started on 2003-04. Estimated completion is 2009-01.

What conditions does trial NCT00223405 study?

This clinical trial studies the following conditions: Tooth Wear.

What interventions are being tested in trial NCT00223405?

The interventions under investigation include: crown placement (DEVICE).

Who is sponsoring clinical trial NCT00223405?

This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00223405 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

  • NCT00929006 · 36 participants · Early Phase 1

    Acute Progesterone Suppression of Wake vs. Sleep Luteinizing Hormone Pulse Frequency in Pubertal Girls With and Without Hyperandrogenism

  • NCT01891318 · 36 participants · Phase 1

    Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study

  • NCT02291848 · 36 participants · Phase 1

    Tumor-Associated Antigen-Specific Cytotoxic T-Lymphocytes for Multiple Myeloma

  • NCT02366819 · 36 participants · Phase 4

    Genetic Analysis-Guided Irinotecan Hydrochloride Dosing of mFOLFIRINOX in Treating Patients With Locally Advanced Gastroesophageal or Stomach Cancer

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

Source: ClinicalTrials.gov NCT00223405, the US trial registry maintained by the National Library of Medicine. NCT00223405 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.