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.

The University of Texas System (UT)

Status: Not yet enrolling

Conditions: Root Canal Treatment

Treatments: Device: GentleWave

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04105907

HSC-DB-19-0476

Details and patient eligibility

About

The purpose of this study is to understand and learn better the efficacy of GentleWave and obtain histological evidence of the efficacy of this new technology done in-vivo

Enrollment: 50 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Partial root canal treatment with the Sonendo GentleWave

Experimental group

Treatment:

Device: GentleWave