NCT07041736 Evaluating Postoperative Pain and Antibacterial Effect of Ultrasonic and 980 nm Diode Laser Combination
| NCT ID | NCT07041736 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Al-Azhar University |
| Condition | Post Operative Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 120 participants |
| Start Date | 2025-08-03 |
| Primary Completion | 2026-04-15 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 120 participants in total. It began in 2025-08-03 with a primary completion date of 2026-04-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * Patients have mature teeth with closed apex. * Single-rooted teeth with root canal form type I. * Asymptomatic. * Have periapical radiolucency with a diameter of up to 5 mm. * Restorable teeth. Exclusion Criteria: * Patients with symptomatic apical periodontitis. * Systemic disease. * Physical or mental disability. * Root fracture and tooth mobility.
Contact & Investigator
Sabah M. Sobhy, PHD
PRINCIPAL INVESTIGATOR
Endodontic Department, Faculty of Dental Medicine for Girls, Al-Azhar University, Cairo, Egyp
Frequently Asked Questions
Who can join the NCT07041736 clinical trial?
This trial is open to participants of all sexes, aged 20 Years or older, up to 35 Years, studying Post Operative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07041736 currently recruiting?
Yes, NCT07041736 is actively recruiting participants. Contact the research team at sabamorad@yahoo.com for enrollment information.
Where is the NCT07041736 trial being conducted?
This trial is being conducted at Cairo, Egypt.
Who is sponsoring the NCT07041736 clinical trial?
NCT07041736 is sponsored by Al-Azhar University. The principal investigator is Sabah M. Sobhy, PHD at Endodontic Department, Faculty of Dental Medicine for Girls, Al-Azhar University, Cairo, Egyp. The trial plans to enroll 120 participants.