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Study identifier: NCT07041736 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluating Postoperative Pain and Antibacterial Effect of Ultrasonic and 980 nm Diode Laser Combination

Condition: Post Operative Pain  ·  Sponsor: Al-Azhar University

PhaseNA
Planned participants120
Who can joinAll sexes, 20 Years to 35 Years
Healthy volunteersNo

About this study

This study is a parallel randomized controlled clinical trial that was designed and interpreted according to Preferred Reporting Items for Randomized Trial in Endodontics (PRIRATE) 2020 guidelines. Patients of age range between 20 and 35 years old from the outpatient clinic of Endodontic Department, Faculty of Dental Medicine for Girls, Al-Azhar University will participate in this study. These patients have single rooted teeth with necrotic pulp and periapical radiolucency. Patients will be informed about all the study's procedures. They will be included in the study after fulfilling the inclusion criteria and sign an informed consent.Inclusion Criteria: * Patients have mature teeth with closed apex. * Single rooted teeth with root canal form type I. * Asymptomatic. * Have Periapical radiolucency with diameter up to 5 mm. * Restorable teeth. Exclusion Criteria: * Patients with symptomatic apical periodontitis. * Systemic disease. * Physical or mental disability. * Root fracture and tooth mobility.

This description comes directly from the study's public registry record.

Talk to the study team

Sabah M. Sobhy, PHD  ·  +201096529143  ·  sabamorad@yahoo.com

Always discuss trial participation with your own doctor first.

Locations (1)

from the outpatient clinic of Endodontic Department, Faculty of Dental Medicine for Girls, Al-Azhar UniversityCairo, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07041736