Endodontic Inflammation Clinical Trial
Official title:
Comparative Evaluation Of Postoperative Pain After Using Sonic Vibringe Irrigation System Versus Conventional Irrigation In Single Rooted Teeth With Symptomatic Irreversible Pulpitis : A Randomized Clinical Controlled Trial
Verified date | August 2019 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Vibringe is the first endodontic sonic irrigation system that enables delivery and
activation of the irrigation solution in the root canal, in only one step. The activation of
the disinfectant by acoustic streaming, enriches and completes the irrigation procedure and
improves the success rate of endodontic treatments. It has been shown that this system
significantly improves debridement. It also improves the disruption of the smear layer and
biofilm by activating irrigation solutions.
As there are no previous studies comparing the Vibringe system with other irrigation
techniques under clinical settings, in this regard, the aim of this study is to evaluate
whether irrigation with Vibringe provides more or less benefit in terms of postoperative pain
when compared with the conventional needle technique.
Status | Completed |
Enrollment | 18 |
Est. completion date | February 28, 2019 |
Est. primary completion date | January 27, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Age between 25-45 years old. - Males or Females. - Single rooted teeth with: - Symptomatic irreversible pulpitis . - Normal periapical radiographic appearance or slight widening in lamina dura. Exclusion Criteria: - Patients on medication for chronic pain. - Patients having significant systemic disorders. - Teeth that have : - Vital pulp tissues. - Swelling or fistulous tract - Acute or chronic peri-apical abscess - Greater than grade I mobility - Pocket depth greater than 5mm - No possible restorability - Previous endodontic treatment. |
Country | Name | City | State |
---|---|---|---|
Egypt | Cairo university | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain intensity ( post operative pain ) | post operative pain measured by Numeric Rating Scale (0-10) where; 0; No pain. 1-3; Mild Pain 4-6; Moderate Pain 7-10; Severe pain: "severe pain, analgesic had no effect in relieving the pain". | 6 hours post- obturation. | |
Primary | pain intensity ( post operative pain ) | post operative pain measured by Numeric Rating Scale (0-10) where; 0; No pain. 1-3; Mild Pain 4-6; Moderate Pain 7-10; Severe pain: "severe pain, analgesic had no effect in relieving the pain". | 12 hours post- obturation. | |
Primary | pain intensity ( post operative pain ) | post operative pain measured by Numeric Rating Scale (0-10) where; 0; No pain. 1-3; Mild Pain 4-6; Moderate Pain 7-10; Severe pain: "severe pain, analgesic had no effect in relieving the pain". | 24 hours post- obturation. | |
Primary | pain intensity ( post operative pain ) | post operative pain measured by Numeric Rating Scale (0-10) where; 0; No pain. 1-3; Mild Pain 4-6; Moderate Pain 7-10; Severe pain: "severe pain, analgesic had no effect in relieving the pain". | 48 hours post- obturation. |
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