Trials / Completed
CompletedNCT06129643
Efficacy of Lasers in Root Canal Treatment, Part II: Postoperative Pain
Efficacy of 2780 nm Er,Cr:YSGG and 940 nm Diode Lasers in Root Canal Treatment, Part II: Postoperative Pain
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- Future University in Egypt · Academic / Other
- Sex
- All
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study is to evaluate in vivo the post operative pain after laser root canal treatment in necrotic teeth in an evidence-based clinical trial. The null hypothesis being tested is that there is no difference in post operative pain between conventional irrigation and the two types of lasers used. Forty-five patients are equally divided into 3 separate groups : * Group A (Conventional): 2.5% NaOCL and 17% EDTA. * Group B(Dual): saline along with Er,Cr:YSGG laser and diode laser combination * Group C(Combined): saline along with 17% EDTA and diode laser combination Each patient is given pain scale chart Numeric Rating Scale (NRS) to record his/her pain level before any endodontic treatment. All data will be collected, tabulated, summarized, and statistically analyzed.
Detailed description
Postoperative pain is a common complication following conventional endodontic treatment. According to a systematic review, the frequency of endodontic postoperative pain is between 3% and 58% of patients.Postoperative pain is attributed to chemical, mechanical and microbiological factors. Residual microorganisms remaining due to the complexity of the root canal system and the limited penetration capability of conventional irrigants are directly responsible for Post operative pain The aim of this study is to evaluate in vivo the post operative pain after laser root canal treatment in necrotic teeth in an evidence-based clinical trial. The null hypothesis being tested is that there is no difference in post operative pain between conventional irrigation and the two types of lasers used. Forty-five patients are equally divided into 3 separate groups : * Group A (Conventional): 2.5% NaOCL and 17% EDTA. * Group B(Dual): saline along with Er,Cr:YSGG laser and diode laser combination * Group C(Combined): saline along with 17% EDTA and diode laser combination Each patient will be given pain scale chart (NRS scale) to record his/her pain level before any endodontic treatment. After disinfection, local anesthetic, tooth isolation, access cavity preparation and final obturation. Patients are asked to mark on a numeric rating scale (NRS) to determine incidence of postoperative pain and rate its intensity at 6, 12, 24, 48, 72 hours, and 7 days after the procedure All data will be collected, tabulated, summarized, and statistically analyzed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Conventional group | conventional disinfection using 2.5% sodium hypochlorite and 17% EDTA |
| DEVICE | Dual laser group | Er,Cr:YSGG intracanal laser irradiation to remove smear layer followed by diode laser for disinfection |
| COMBINATION_PRODUCT | Combined group | 17% EDTA was used to remove smear layer followed by diode laser for disinfection |
Timeline
- Start date
- 2022-01-01
- Primary completion
- 2022-10-30
- Completion
- 2023-02-01
- First posted
- 2023-11-13
- Last updated
- 2026-03-11
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06129643. Inclusion in this directory is not an endorsement.