Health Condition 1: K053- Chronic periodontitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Systemically healthy patient. 2)Patient age ranging 25-60 years. 3)Periodontal pocket depth more than or equal to 5mm. 4)Patient requiring at least 2 quadrants for flap surgery. 5)Patients with good oral hygiene after scaling and root planning. 6)Presence of at least 20 natural teeth. 7)Patient willing to participate in the study.
Exclusion criteria
Exclusion criteria: 1)The patients who are undergoing treatment with analgesics or corticosteroids during the trial period. 2)Pregnancy and lactating mothers. Smokers and alcoholic. 3)Patients with cardiovascular disease. 4)Patients with gastrointestinal bleeding or ulcers. 5)Patients with liver diseases. 6)Patients with kidney diseases. 7)Patient allergic to Diclofenac and Ketoprofen.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare and evaluate the efficacy of Ketoprofen and Diclofenac transdermal patch in the management of postoperative pain following periodontal flap surgery.Timepoint: Every hour upto 8hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To evaluate the efficacy of Diclofenac transdermal patch in reducing postoperative pain following periodontology flap surgery. 2)To evaluate the efficacy of Ketoprofen transdermal patch in reducing postoperative pain following periodontology flap surgery. 3)To compare the efficacy of Ketoprofen and Diclofenac transdermal patch in reducing postoperative pain following periodontal flap surgery. 4)To evaluate the adverse reaction (if any) following the use of Diclofenac and Ketoprofen transdermal patch. Timepoint: Every hour upto 8hours | — |
Countries
India
Contacts
KVG Dental College and Hospital