Dental Pulp Necrosis Clinical Trial
Official title:
Comparison of Postoperative Pain After Root Canal Instrumentation Using Reciproc and ProTaper Next in Asymptomatic Necrotic Molars: A Randomized Clinical Trial
Verified date | November 2017 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Comparing the postoperative pain resulting after mechanical instrumentation using Reciproc reciprocating files versus that resulting after using ProTaper Next rotary files in asymptomatic necrotic molars.
Status | Completed |
Enrollment | 60 |
Est. completion date | November 2017 |
Est. primary completion date | October 14, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 15 Years to 55 Years |
Eligibility |
Inclusion Criteria: - Mandibular molar teeth with no pain, no response of pulp tissue to pulp testing and teeth with apical periodontitis Exclusion Criteria: - Patients on medication for chronic pain - Patients with pre-operative pain. - Patients having significant systemic disorders. - Patients with two or more adjacent teeth requiring root canal therapy - teeth that have vital pulp tissues, greater than grade I mobility, pocket depth greater than 5 mm, no possible restorability or previous endodontic treatment. |
Country | Name | City | State |
---|---|---|---|
Egypt | Cairo university | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Bürklein S, Schäfer E. Apically extruded debris with reciprocating single-file and full-sequence rotary instrumentation systems. J Endod. 2012 Jun;38(6):850-2. doi: 10.1016/j.joen.2012.02.017. Epub 2012 Apr 6. — View Citation
Nekoofar MH, Sheykhrezae MS, Meraji N, Jamee A, Shirvani A, Jamee J, Dummer PM. Comparison of the effect of root canal preparation by using WaveOne and ProTaper on postoperative pain: a randomized clinical trial. J Endod. 2015 May;41(5):575-8. doi: 10.1016/j.joen.2014.12.026. Epub 2015 Feb 24. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Post operative pain assessed with the Numerical Rating Pain Scale | 1 to 10 Numerical Rating Pain Scale up to 48 hours post-instrumentation | Up to 48 hours post-instrumentation | |
Primary | Post-obturation pain assessed with the Numerical Rating Pain Scale | 1 to 10 Numerical Rating Pain Scale up to 24 hours following obturation | up to 24 hours following obturation | |
Secondary | Time required to complete instrumentation | time required to complete instrumentation | From the completion of the access cavity preparation till the end of cleaning and shaping procedure up to 2 hours |
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