Not Yet RecruitingNot Applicable

Effectiveness of GentleWave System in Endodontic Treatment

United States70 participantsStarted 2024-08-20

Plain-language summary

This study aims to evaluate the efficacy of the GentleWave® System compared to conventional methods in reducing postoperative pain in patients with necrotic pulp or requiring endodontic retreatment.

Who can participate

Age range18 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male and female patients from 18 years age or older (maximum of 80 years of age), both genders. * The patients in need of an endodontic intervention. * All dental groups in both arches were eligible. * Patients who do or do not experience symptoms after the endodontic intervention. * Patient-signed informed consent/assent form Exclusion Criteria: * Patients\< 18 years old. * fractured teeth. * Patients who were recommended extraction after the endodontic evaluation.

What they're measuring

To evaluate whether using the Gentlewave system demonstrates a significant reduction in the level of postoperative pain after endodontic treatment measured by the VAS (Visual Analog Scale).

Timeframe: 24 hours

Trial details

NCT IDNCT06518304

SponsorUniversity of Salamanca

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-20

View on ClinicalTrials.gov More Pain, Postoperative trials