Overview

Premedication Efficacy of Oral Ketorolac and Ketorolac/ Acetaminophen on Post Treatment Pain

Status:
Completed
Trial end date:
2016-05-01
Target enrollment:
0
Participant gender:
All
Summary
The aim of this study is premedication efficacy of analgesics on post endodontic pain. Sixty-six healthy adult volunteers including criteria, are participating. The patients will be divided into 3 groups and will be randomly given one of pre medications including 1) 10 mg Ketorolac, 2) 10 mg Ketorolac plus 1000mg Acetaminophen, and 3)Placebo, 45 minutes before applying the injection. All patients will receive standard root canal treatment. Patients will record their post treatment pain using a Heft parker Visual Analog Scale(VAS). Success will be considered as no or mild pain (VAS≤54)with no need to take analgesic. Data will be analysed using Mann-U-Whitney and Kruskal-wallis tests.
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Azad University of Medical Sciences
Treatments:
Acetaminophen
Ketorolac
Ketorolac Tromethamine
Criteria
Inclusion Criteria:

- Patients with age ranged 18-65

- without systemic diseases

- without any medicine consumption

- non smoking

- non pregnant

- non breast feeding

- with asymptomatic irreversible pulpitis ( Visual Analog Scale ≤ 54) in one mandibular
molar that needs root canal treatment

- without any medicine consumption or analgesic and sedation who understand and sign the
VAS and consent forms.

Exclusion Criteria:

-