A Clinical Trail to Compare the efficacy of transdermal patch of diclofenac and ketoprofen for treatment of post endodontic pain control
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/06/054464
- Lead Sponsor
- PANINEEYA INSTITUTE OF DENTAL SCIENCES
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
i) Patients belonging to both sexes between the age group of 18 and 45
years
ii) Patients complaining of pain in single-rooted teeth of either jaw and
diagnosed as symptomatic irreversible pulpitis.
iii) Selected teeth should show intact lamina dura in intraoral periapical
radiograph with no periapical radiolucency and absence of
anatomical obstacles such as calcifications in the canals with no
anticipated procedural difficulties.
iv) Patients who give informed consent for the study
i) Patients with hypersensitivity against diclofenac.
ii) Patients with a history of allergic reactions such as bronchospasm,
shock, urticarial, etc., following the use of diclofenac or other
non-steroidal anti-inflammatory drugs (NSAIDs).
iii) Patients with active stomach or duodenal ulceration within the last 6
months.
iv) Patients undergoing treatment with other NSAIDs or corticosteroids
during the study period.
v) Patients with a history of systemic diseases such as bronchial
asthma, epilepsy, inflammatory bowel disease, severe liver or renal
insufficiency, dengue fever, emotional and psychosomatic
disorders.
vi) Pregnant and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method