Health Condition 1: null- The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception.
Conditions
Interventions
Intervention1: preoperative ketarolac: the patients shall receive orally 10 mg of ketarolac 1hr before the treatment
Control Intervention1: preoperative paracetamol: The patients shall orally receive
Sponsors
Faculty of Dentistry JMI
Eligibility
Inclusion criteria
Inclusion criteria: The subjects should be actively experiencing pain and in good health, and none will be taking any medication that would alter pain perception, as determined by oral questioning and written questionnaire.
Exclusion criteria
Exclusion criteria: Cardiac patients, pregnant patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success will be defined as no pain or weak/mild pain during endodontic access preparation and instrumentationTimepoint: The primary outcome shall be measured during the root canal procedures. | — |
Secondary
| Measure | Time frame |
|---|---|
| Success will be defined as no pain or weak/mild pain during endodontic accessTimepoint: The secondary outcomes shall be measured during endodontic access preparation and instrumentation | — |
Countries
India
Contacts
Public ContactDr Vivek Aggarwal
Faculty of Dentistry, Jamia Millia Islamia
Outcome results
None listed