Inflammation Clinical Trial
Official title:
Efficacy Evaluation of the Dose Regimen of Serratiopeptidase (Serodase 5 mg Tablet) in the Treatment of Inflammation After Third Molar Surgery
The purpose of this study is to examine the efficacy of dose regimen of serratiopeptidase (serodase 5 mg) as a prospective, randomized, parallel, double blind Placebo- controlled study.
A prospective, randomized, parallel, double blind Placebo- controlled study to examine the
efficacy of dose regimen of serratiopeptidase (serodase 5 mg) on 112 males and females
volunteers in the treatment of inflammation after third molar surgery, comparing drug
treatment vs placebo over a period of 20 weeks To assess the dose effectiveness of the dose
regimen of Serodase 5 mg; the primary outcomes are trismus and swelling while inflammation
is a secondary outcome.the expected duration of participants participation will be around 5
days divided into 4 visits, the time point of the measurment are (0,2,4 and 5 days).
The results are expected to assess the improvement of the maximal interincisal distance,
reduction of swelling and improvment in the sensation of post-operative pain.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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