Symptomatic Periapical Periodontitis Clinical Trial
Official title:
Effect of Preoperative Single-dose Clindamycin on Postoperative Endodontic Pain in Patients With Symptomatic Apical Periodontitis: A Randomized Controlled Trial
The aim of this prospective, randomized, placebo controlled study is to evaluate the effect of clindamycin on post-operative pain and swelling in adult patient with symptomatic apical periodontitis.
Medical and dental history will be obtained from all patients participating in this trial.
Clinical and radiographic evaluation for each tooth included in this study will be recorded.
Clinical diagnosis of symptomatic apical periodontitis is to be confirmed.
Before root canal treatment, eligible participants will be randomly assigned to one of the
following groups: experimental group (taking 600 mg of clindamycin orally) or control group
(taking placebo ) 30 minutes before the start of the treatment. Single-visit root canal
treatment will be performed.
Each patient will receive a 7-day diary to record postoperative pain and swelling.In case of
pain, the participant will be instructed to take an analgesic. Post-operative pain will be
measured as a primary outcome on 11-point scale (NRS) at the following time points: 6, 12,
24, 48, 72 hours and 7 days. The occurrence of swelling will be reported by participant as a
secondary outcome
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