Evaluating the effectiveness of GentleWave technology in root canal treatment
Histological Evaluation in the Efficacy of GentleWave in Root Canal Pulp Tissue Debridement and Disinfection of Difficult to Reach Areas in Mandibular Human Molars II. An In-vivo Study.
This study is testing if the GentleWave system can clean and disinfect hard-to-reach areas in molars to help patients who are considering tooth extraction.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | The University of Texas Health Science Center, Houston Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT04105907 on ClinicalTrials.gov |
What this trial studies
This study aims to assess the efficacy of the GentleWave system in debriding and disinfecting pulp tissue in difficult-to-reach areas of mandibular molars. It will involve in-vivo histological evaluations to gather evidence on the effectiveness of this innovative technology. The study focuses on teeth that patients have opted to extract rather than pursue other dental treatments, ensuring a specific patient population for analysis.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have chosen to extract their teeth instead of undergoing other dental treatments.
Not a fit: Patients with root fractures, previously treated root canals, or severe structural loss of teeth will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve root canal treatment outcomes and patient experiences by providing a more effective disinfection method.
How similar studies have performed: While the GentleWave technology is relatively novel, similar studies have shown promising results in improving root canal treatment efficacy.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Only teeth that patient decided to have the extraction done instead of having any other type of dental treatment and teeth extracted at patient's petition. Exclusion Criteria: * Teeth with root fractures or previously root canal treated teeth. * Teeth with severe loss of structure * Children
Where this trial is running
Houston, Texas
- The University of Texas Health Science Center at Houston — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: David E Jaramillo, DDS — The University of Texas Health Science Center, Houston
- Study coordinator: David E Jaramillo, DDS
- Email: David.E.Jaramillo@uth.tmc.edu
- Phone: 713-486-4221
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.