Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with BILATERAL SYMMETRICAL MAXILLARY OR MANDIBULAR teeth indicated for extraction. 2.Patients undergoing intra-alveolar extraction within 10 minutes duration.
Exclusion criteria
Exclusion criteria: 1. Patients with known allergy to NSAIDS. 2. Pregnant women. 3. Patients on any other analgesics or corticosteroids. 4. Patients with history of systemic diseases like bronchial asthma, epilepsy, and emotional and psychosomatic disorders. 5. Patients unwilling to consent for the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The benefit is it helps determine the optimal route for diclofenac delivery based on factors like bioavailability and patient tolerance. Timepoint: Pain will be assessed for 7 days regularly and will be recorded Healing will be recorded at 7 days post extraction | — |
Secondary
| Measure | Time frame |
|---|---|
| The need for the current study is to examine and assess efficacy of diclofenac gel foam placed in extraction sockets as an alternative to oral analgesic. Timepoint: 6 months | — |
Countries
India
Contacts
Yenepoya Dental College