Post Operative Pain
Conditions
Brief summary
conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers
Detailed description
STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS. TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS, GROUP1: ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS. GROUP2: ALL CANALS WILL BE OBTURATED USING HIGH FLOW BIOCERAMIC SEALERS THAT ACCEPT WARM VERTICAL COMPACTION POST OPERATIVE PAIN IN THE TWO GROUPS WILL BE EVALUATED USING THE VISUAL ANALOUG SCALE AND COMPARED AT DIFFERENT TIME PERIODS (12H, 24H, 48H, 72H)
Interventions
OTHERroot canal sealers
different sealer used in obturating root canals (resin and bio ceramic)
Sponsors
British University In Egypt
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Patients were randomly divided into two groups according to material used for obturation . each patients name will be replaced with a case number within the group to protect the privacy of medical information and data of the patients care provider and the investigator will not know the name of the patient and the assessor doesn't know the group he is assessing
Intervention model description
randomized clinical trial
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* • Patients age ranges from 18-50 years old. * Patients with teeth diagnosed with symptomatic irreversible pulpitis. * Normal periapical condition confirmed by normal periapical radiograph or that with minimal widening of the PDL space * The teeth are restorable * Teeth are periodontally free.
Exclusion criteria
* • Teeth with immature roots * Non restorable teeth * Medically compromised patients with systemic complication that would alter the treatment. * Necrotic teeth * Teeth with apical periodontitis or periapical lesions * Teeth that need multiple visits treatment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 12 hours | 12 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 24 hours | 24 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 48 hours | 48 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 72 hours | 72 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. |
Countries
Egypt
Contacts
Primary Contactsara tarek mohamed, bachelor
Backup Contacthala F khalil, lecturer
Outcome results
None listed