CTRI/2024/02/062947RecruitingPhase 4
Comparative evaluation of efficacy of single pre-emptive dose of Extended release Lornoxicam versus Prolonged release Diclofenac for surgical removal of impacted 3rd molar in Indian population: A prospective, randomized, triple blind, split mouth clinical trial. - NI
Trial Snapshot
- Phase
- Phase 4
- Status
- Recruiting
- Sponsor
- Terna Dental College
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Patients who are willing to participate in the study
- •2.Patients requiring surgical extraction of bilateral impacted mandibular 3rd molar of similar difficulty (easy or moderate difficulty as per Pederson’s difficulty index)
- •3.Healthy patients belonging to ASA Class I or II will be included
- •4.Patients who are not on any pain management therapy or those who have not consumed any NSAID in the last seven days.
Exclusion Criteria
- •1.Patients not willing to participate in the study
- •2.H/o Hypersensitivity reactions to Lornoxicam, Diclofenac or any other NSAID
- •3.Pregnant and lactating patients
- •4.Patients suffering from Bronchial Asthma or COPD or bleeding diathesis.
- •5.Patients with H/o gastritis, gastric/ duodenal ulcers, or any other inflammatory gastrointestinal disease
- •6.Pederson difficulty index score 7-10 (Difficult)
- •7.Patients having local signs of infection around the impacted tooth to be removed such as periapical abscess/granuloma, pericoronal abscess, fascial space infection etc.
Investigators
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