A clinical study to compare pain reduction effect of diclofenac sodium mouthwash with diclofenac sodium tablet after gum surgery; a pilot study.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients indicated for periodontal surgeries.
- Registration Number
- CTRI/2018/01/011365
- Lead Sponsor
- none
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
1.Systemically healthy patients.
2.Patients indicated for periodontal surgeries.
Exclusion Criteria
1.Patients with the history of intolerance or hypersensitivity to diclofenac.
2.Any systemic diseases or condition that affects the oral tissues,
3.Pregnant or lactating women.
4.Patients on oral/systemic NSAIDs therapy for the last three months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Topical formulation of diclofenac sodium will be sufficiently effective for pain relief after periodontal surgical procedures when compared to systemic formulation of diclofenac sodium.Timepoint: Analgesic effect will checked on 1st 2nd 3rd and 4th day after surgery by NRS index.
- Secondary Outcome Measures
Name Time Method noneTimepoint: none