Pre-Emptive Analgesic Effect of Tramadol After Mandibular Third Molar Extraction: A Pilot Study
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Purpose: We compared the efficacy of tramadol given before or immediately after surgical extraction of an impacted mandibular third molar under local anesthesia. Materials and Methods: In this prospective, randomized, controlled, double-blind pilot study, 3 groups of 20 patients each were included: tramadol preoperative, 100 mg intramuscularly (IM) 1 hour before surgery (group A); tramadol postoperative, 100 mg IM immediately after surgery (group B); and saline (group C). We evaluated intensity of pain and analgesic consumption as was requested. Results: The analgesic efficacy measured as complete relief of pain at 24 hours was 86%25 in the preemptive tramadol compared with 70%25 and 36%25 for postoperative tramadol administration and control group. A significant reduction in the consumption of analgesics was seen in preoperative group as compared with the postoperative and control groups. Adverse events were minimal and similar in all groups. Conclusions: This study suggests the preemptive use of tramadol as an alternative for the acute pain treatment after the removal of an impacted mandibular third molar carried out under local anesthesia. © 2007 American Association of Oral and Maxillofacial Surgeons.
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dexamethasone; ketorolac; paracetamol; sodium chloride; tradol; tramadol; unclassified drug; adult; analgesia; article; clinical article; clinical trial; controlled clinical trial; controlled study; double blind procedure; drug effect; drug efficacy; female; human; male; molar tooth; operation duration; pain; prophylaxis; randomized controlled trial; tooth extraction; unspecified side effect; Adult; Analgesics, Opioid; Double-Blind Method; Female; Humans; Injections, Intramuscular; Male; Mandible; Molar, Third; Pain Measurement; Pain, Postoperative; Pilot Projects; Postoperative Care; Preanesthetic Medication; Statistics, Nonparametric; Tooth Extraction; Tooth, Impacted; Tramadol
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