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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04311905
Other study ID # END 16-15D
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2017
Est. completion date January 1, 2020

Study information

Verified date March 2020
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study is a Randomized clinical trial conducted at Endodontic department- Ain Shams university Cairo. Egypt. 24 eligible patients were selected and included in the study to compare healing ability of diode laser activated irrigation versus conventional root canal treatment using CBCT


Description:

Sample size is 24 , 24 Patients were randomly distributed in 2 groups , one group of patients received laser activated irrigation LAI during root canal treatment and the other group received no treatment just conventional RCT. • Patients were equally divided into 2 groups (n=12 in each group ) The study in a Single blinded RCT , Numbers for patients will be generated and distributed randomly in a table on an Excel sheet, and in front of each number either a letter (C) for control or (I) for intervention will be typed After patients were selected in the study they will be asked to fill in a consent form , that states that they are part of a clinical trial and that they may or may not receive a laser activated irrigation Group A LAI :Disinfection were done by using 5 ml of 2.5% sodium hypochlorite irrigation for 1 minute. Irrigation will be performed with a 30-gauge needle side vented The irrigation needles were introduced passively up to 2 mm away the working length. After irrigation Laser treatment will be performed with a diode laser, at a wavelength of 980 nm with a repeated pulse mode using a pulse duration of 5sec per canal and a pulse interval of 0.2 ms. The laser irradiation were delivered for 1 minute into the canal up to 1 mm short of the working length, with circling movements from the apical part moving towards the coronal part Group B : received mock laser intervention , conventional Root canal treatment with 2.5% sodium hypochlorite CBCT was taken pre-operative and another one was taken after 12 month , both volumetric and linear measurements were calculated


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date January 1, 2020
Est. primary completion date July 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Adult patients age between 18-50 years

- Medically free patients.

- Patients suffering from acute or chronic infection with symptomatic apical periodontitis with Necrotic pulp

- Preoperative Pain

- Sensitivity to percussion

- Periapical radiographic X-ray showing periapical lesion with no gutta percha in canal

- Occlusal contact with opposing teeth

Exclusion Criteria:

- Pregnant females.

- Patients having a significant systemic disorder or history of drug abuse

- Patients who had administrated analgesics or antibiotics during the last 12 hours preoperatively.

- Patients having bruxism or clenching

- Teeth having:

- No occlusal contact

- No sensitivity to percussion

- Greater than grade I mobility.

- Pocket depth greater than 5mm.

- No possible restorability

- Procedural errors

- Previous Root canal treatment

- Open apex

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Diode laser
Diode laser activated irrigation
Other:
Placebo
mock Laser activated irrigation

Locations

Country Name City State
Egypt Endodontic department - Faculty of Dentistry Ainshams University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess post-operative healing using CBCT in a period of 12 month when Laser activated irrigation was used during root canal treatment 12 months
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