Pulp Necrosis Clinical Trial
Official title:
Evaluation of Success Rate of Non Vital Mature Anterior Teeth With Periapical Lesion Following Single Versus Two Visit Regenerative Treatment Protocol A Randomized Clinical Study
Verified date | October 2018 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates success rate of non vital mature anterior teeth with periapical lesion
treated by regenerative endodontic protocol in single visit versus two visit technique.
Patients are randomized into two groups where treatment will be done either in one visit
including access, disinfection, placing platelet rich plasma as scaffold and restoration or
two visit protocol involving access, disinfection and placing calcium hydroxide as intracanal
medicament in first visit followed by a second visit after 3 weeks involving reopening of the
tooth, removing intracanal medicament and placing platelet rich plasma as scaffold then
restoration. Success rate is defined as absence of subjective signs and symptoms along with
healing of periapical lesion
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | December 1, 2020 |
Est. primary completion date | September 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 15 Years to 35 Years |
Eligibility |
Inclusion Criteria: - Single canal anterior tooth - Mature root - Non vital with radiographic evidence of periapical lesion - Periapical lesion of average size 2-5mm - Positive patient compliance for participation in the study. - Patients with good oral hygiene - Normal periodontal probing depth = 3 mm Exclusion Criteria: - Compromised remaining tooth structure that need post and core build up - Non restorable teeth - Vital teeth - Radiographic evidence of external or internal root resorption. - Roots showing fracture or ankylosis - Medically compromised patients - Pregnant women - Greater than grade I mobility or periodontal probing depth greater than 3mm - Immature tooth - Patients with pain, swelling or fistula tracts |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Post operative pain: NRS | absence of pain reported by the patient by numerical rate scale, the 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") | 3, 6, 9 and 12 months | |
Primary | Change in swelling and/or sinus | The presence of swelling or sinus will be reported by a binary question yes/no | 3,6,9,12 months | |
Primary | Periapical healing | The existing periapical lesion will be measured by mm by CBCT before intiation of treatment and after one year | 12 months | |
Secondary | Antimicrobial effect | intracanal bacterial count by culture method | before and after complete disinfection either in the same visit or after 3 weeks from the second visit | |
Secondary | Sensitivity | Tooth giving respond to electrical pulp tester | 3, 6, 9 and 12 months | |
Secondary | Discoloration | Recording tooth shade before and after treatment | 3, 6, 9 and 12 months |
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