Overview

Dexketoprofen Trometamol in Postoperative Endodontic Pain

Status:
Completed
Trial end date:
2014-04-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to investigate the analgesic efficacy of multiple doses of Dexketoprofen Trometamol 25 mg on postoperative pain following emergency endodontic treatment in teeth with irreversible pulpitis, using as control Ibuprofen 600 mg and a placebo group. Hypothesis: Dexketoprofen trometamol when administered in multiple doses produces a greater effect to control postoperative pain after treating symptomatic irreversible pulpitis; in patients undergoing pulpotomy as an emergency procedure
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Daniel Chavarría Bolaños
Treatments:
Dexketoprofen trometamol
Ibuprofen
Ketoprofen
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)