postoperative pain after non-
Conditions
Interventions
using solvent (GuttaClear) in procedure ,not using solvent (GuttaClear) in procedure
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
solvent,non-
Sponsors
Faculty of Graduate Studies
Faculty of Graduate Studies
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Participants aged more than 18 years with healthy physical status or well-controlled systematic diseases, according to class I or II from ASA classification will be enrolled. In addition, they should not be contra-indicated with medication used in this study (ibuprofen), i.e., drug allergy or related systemic conditions. All included participants will have a previously treated endodontic single-root tooth with the need of retreatment and all those teeth must be restorable. Moreover, old root canal filling materials must be located at 1 to 3 mm from the radiographic apex in the periapical radiograph.
Exclusion criteria
Exclusion criteria: Any tooth presenting an open apex, root resorption or root perforation would be excluded. In addition, participants presenting pre-operative pain and/or swelling at the appointment visit, taking analgesics or antibiotics less than one week before appointment visit or experiencing problems in completing the pain questionnaires would be excluded. Moreover, a tooth which does not contain gutta-percha or cannot be patent through the apex at the appointment visit will be excluded, too.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative pain 3 days NRS score | — |
Secondary
| Measure | Time frame |
|---|---|
| the amount of medication intake 3 days number | — |
Countries
Thailand
Contacts
Public ContactDuangrat Sirijindamai
Mahidol University
Outcome results
None listed