Dexketoprofen Trometamol in Postoperative Endodontic Pain (DTPEP)
Irreversible Pulpitis
About this trial
This is an interventional treatment trial for Irreversible Pulpitis focused on measuring pain, symptomatic irreversible pulpitis, postoperative dental pain
Eligibility Criteria
Inclusion Criteria:
- Subjects aged 18 years and older with moderate-to-severe dental pain assessed by numerical rating scale (NRS) associated with irreversible pulpitis.
Exclusion Criteria:
• Female pregnant or breastfeeding
- Used pain relievers or anti-inflammatory drugs within 24 hours preceding emergency endodontic treatment
- Have any significant medical condition
- Taking any medications for anxiety, depression or schizophrenia
- Have a history of hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs)
Sites / Locations
- Endodontics Master Degree program, Dentistry Faculty, San Luis Potosi University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Placebo Comparator
dexketoprofen trometamol
IBUPROFEN
PLACEBO
Administration of 25mg of Dexketoprofen Trometamol, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed
Administration of 600mg of Ibuprofen, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed
4 doses of sugar pills, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed