Periapical Diseases Clinical Trial
Official title:
Efficiency of Diode Laser in Control of Post-endodontic Pain (A Randomized Clinical Trial )
NCT number | NCT04315259 |
Other study ID # | END 16-13D |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 1, 2017 |
Est. completion date | January 1, 2020 |
Verified date | March 2020 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Study is a Randomized clinical trial conducted at Endodontic department- Ain Shams university
Cairo. Egypt.
180 eligible patients were selected and included in the study to assess the post-endodontic
pain of diode laser activated irrigation versus soft tissue diode laser application post
obturation versus conventional root canal treatment .
Status | Completed |
Enrollment | 180 |
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 |
Country | Name | City | State |
---|---|---|---|
Egypt | Endodontic department - Faculty of Dentistry Ainshams University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measure change in post-operative pain after Laser intervention using a visual analogue scale (VAS) questionnaire where 0 indicates no pain and 10 indicates severe pain | 24 hours | ||
Primary | Measure change in post-operative pain after Laser intervention using a visual analogue scale (VAS) questionnaire where 0 indicates no pain and 10 indicates severe pain | 48 hours | ||
Primary | Measure change in post-operative pain after Laser intervention using a visual analogue scale (VAS) questionnaire where 0 indicates no pain and 10 indicates severe pain | 72 hours |
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