RECRUITING

Miniscrew Stability and Peri-implant Inflammation When Precoated K21 vs Ethanol Control

Talk to us

Conditions

Inflammation Caused by the Placement of a Temporary Anchorage DeviceTADinflammationorthodontics

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To determine if coating miniscrews with K21 would increase the success rate of orthodontic miniscrews by reducing adjacent tissue inflammation.

Official Title

A Comparison of Miniscrew Stability and Peri-implant Inflammation When Precoated With Antimicrobial Quaternary Ammonium Compound K21 vs Ethanol Control in Orthodontic Patients: a Triple-blind, Split-mouth, Randomized Controlled Clinical Trial

Quick Facts

Study Start:2022-11-11
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05639907

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Good general health, with no significant medical findings
  2. 2. Requiring at least two miniscrews in their treatment plans (i.e., most participants will have two miniscrews, but some may receive four or six as indicated by their individual treatment plan)
  3. 3. Miniscrew pairs indicated with comparable anatomical positions and comparable mechanics (direct vs. indirect anchorage).
  1. 1. Recent or ongoing use of antiresorptive pharmacological agents contraindicating the use of orthodontic miniscrews
  2. 2. Less than 12 years of age
  3. 3. Heavy tobacco use (\>10 cigarettes/day)
  4. 4. Peri-implant tissues must be observable at follow-up appointments
  5. 5. Being unable or unwilling to consent to the study

Contacts and Locations

Study Contact

Clifton M Carey, PhD
CONTACT
3037241046
clifton.carey@cuanschutz.edu
Gerald Minick, DDS
CONTACT
3037247830
gerald.minick@cuanschutz.edu

Study Locations (Sites)

University of Colorado School of Dental Medicine
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-11-11
Study Completion Date2025-06

Study Record Updates

Study Start Date2022-11-11
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • TAD
  • inflammation
  • orthodontics

Additional Relevant MeSH Terms

  • Inflammation Caused by the Placement of a Temporary Anchorage Device