Laser Activation in Reducing Pain During and After Root Canal Treatment for Painful Lower Molar Teeth.

NCT ID: NCT04735120

Last Updated: 2021-02-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-01
• Study Completion Date: 2022-02-01

Brief Summary

Effectiveness of lasers in reducing pain during and after root canal treatment for mandibular molar teeth affected with acute irreversible pulpitis.

Detailed Description

AIM : To assess the intraoperative and postoperative pain incidence for single visit root canal treatment for mandibular molar teeth with acute irreversible pulpitis following laser activation.

MATERIALS AND METHODS: The study will account the patients who are referred to the Department of Endodontics,both male and female patients,with pain due to acute irreversible pulpitis from carious mandibular first and second molar teeth requiring root canal treatment. Subjects of age 13 to 70 years who met the inclusion criteria and responded positively to cold test will be included in the study.

Single visit root canal treatment with 2.5 mL of 2% lignocaine containing 1:80,000 adrenaline for an inferior alveolar block injection will be administered for each individual. After achieving anesthesia, patients who exhibit pain following access opening will be subjected to diode laser application on the pulp canal orifices. With regard to intraoperative pain, pre laser and post laser intraoperative pain incidence will be recorded. Once when the intraoperative pain incidence is reduced, patients will be reassessed for the need of additional anesthesia. If fully anesthetised, root canal procedure will be completed. Preoperative, intraoperative( before and laser application) pulse rate will also be measured. The levels of preoperative and post-operative pain at 24 hrs and 48 hrs for each patient will be recorded using a 10-point visual analog scale (VAS).

Conditions

Decayed Teeth

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Laser to reduce pain intraoperatively and post operatively

Diode lasers are used to assess its efficacy in reducing intraoperative and postoperative pain following root canal treatment in mandibular molar teeth with acute irreversible pulpitis

Group Type: EXPERIMENTAL

iLASE DIODE LASERS

Intervention Type: DEVICE

940nm diode laser with 1.5 watts activated in a continuous mode and applied on to the canal orifices during root canal treatment to reduce intraoperative pain and further its effect on post operative pain is assessed

Interventions

iLASE DIODE LASERS

940nm diode laser with 1.5 watts activated in a continuous mode and applied on to the canal orifices during root canal treatment to reduce intraoperative pain and further its effect on post operative pain is assessed

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patients with painful mandibular molar teeth due to caries with no history of medication intake before 7 days prior to root canal treatment
• Patients who respond exaggerated pain with or without lingering response on cold test

Exclusion Criteria

• Patients who do not have pain upon access opening following local anesthesia administration
• Teeth with poor periodontal or restorative prognosis,
• Patients with serious systemic ailments or conditions hindering single visit root canal treatment
• patients not willing to participate in the post operative recall evaluation
• Teeth with anatomic variations and
• Allergic patients are excluded

• Minimum Eligible Age: 13 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

CSI College of Dental Sciences and Research, Madurai

OTHER

Sponsor Role: lead

Responsible Party

Dr SUBASHRI V

Principal investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Csi College of Dental Sciences and Research

Madurai, , India

Site Status: RECRUITING

Countries

India

Facility Contacts

SUBASHRI VISWANATHAN, MDS III YEAR

Role: primary

shrimitha26@gmail.com

9445659453

Other Identifiers

CSICDSR

Identifier Type: -

Identifier Source: org_study_id