N/A
N=194
Post-endodontic Pain Survey
Postoperative Pain · Endodontic Disease · Obturation
Bottom Line
View on ClinicalTrials.gov: NCT04462731 ↗Enrolled (actual)
194
Serious AEs
0.0%
Results posted
Jul 2020
Primary outcome: Primary: Visual Analogue Scale (VAS) — 4.06; 2.68; 2.41; 2.27 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Non-surgical root canal treatment filled with WVT (Procedure); Non-surgical root canal treatment filled with SBT (Procedure)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Ya-Hsin Yu, DDS, MS
- Primary completion
- May 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Visual Analogue Scale (VAS) |
4.06; 2.68; 2.41; 2.27; 1.95; 1.8 | — |
Summary
As part of root canal treatment, canals should be sealed to prevent further contaminations. There are multiple accepted techniques to fill-obturate canals. In the past, different obturation techniques have been compared. The most current technique used, a single cone with bioceramic sealer, has not been compared. This clinical investigation will compare the postoperative pain of this technique to another common technique used in our clinic. Postoperative pain after one-visit root-canal treatment on teeth with vital pulps: Comparison of three different obturation techniques.
Eligibility Criteria
Inclusion Criteria
- Diagnosis of asymptomatic or symptomatic irreversible pulpitis according to AAE consensus. The diagnosis was based on clinical examinations and confirmed upon accessing the teeth.
- Consenting adults age 18 years and older
- Non-contributory medical history (ASA Class I & II)
- Included patients were given oral and written information agreed for participation and signed the informed consent
Exclusion Criteria
- Non-consenting patients and patients below 18 years of age
- Medical history with ASA Class III & IV
- Non-restorable teeth
- Teeth with a non-vital pulp
- Periodontal probing depths were more than 4mm
- Pre-medication with antibiotics and/or analgesics 24 hours before the treatment
- Patients taking analgesics routinely for non-dental reasons
Data sourced from ClinicalTrials.gov (NCT04462731). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.