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Termoplastik Kor tekniğini Iki farklı Kanal patı Ile kullanıp Tedavi sonrası Hassasiyet ve kök Ucundan taşma miktarının değerlendirilmesi: Randomize kontrollü Klinik çalışma (NCT03029520)

The aim of this study was to evaluate and compare postoperative pain and overextension of root canal filling after root canal treatment using a carrier-based obturation system and two different sealers. In this prospective randomized clinical trial, 160 mandibular premolars and molars in 160 patients were treated. Patients with vital and devital teeth were assigned to four groups using a randomized block design with block sizes of 10 patients each. The groups were composed of devital teeth with periapical lesions treated with iRoot SP sealer, vital teeth treated with iRoot SP sealer, devital teeth with periapical lesions treated with AH Plus sealer, and vital teeth treated with AH Plus sealer. In single visits, a single operator prepared root canals and filled them with sealer using the carrier-based obturation technique. Radiographs were taken and obturation length was recorded. Patients recorded pain scores use of Visual Analogue Scale and frequency of analgesic intake at baseline and 0-6, 6-12, 12-24, and 24-72 h..
  • Other: Root canal obturation with iRoot SP sealer
    Postoperative pain after root canal obturation with iRoot SP sealer with patients who has (mandibular premolar/molar) vital and devital pulps.
    • Other: Root canal obturation with AH Plus Sealer
      Postoperative pain after root canal obturation with AH Plus sealer with patients who has (mandibular premolar/molar) vital and devital pulps.
      Ages eligible for Study
      18 Years to 65 Years
      Genders eligible for Study
      All
      Accepts Healthy Volunteers
      Accepts Healthy Volunteers
      Inclusion Criteria:
      • no systemic diseases
      • women were not pregnant or breastfeeding status
      • no history of taking analgesics in the previous seven days or other drugs prior to presenting for treatment.
      • all selected teeth were mandibular molar or mandibular premolar.
      Exclusion Criteria:
      • systemic and/or periodontal disease;
      • allergy to local anesthetic agents and/or history of intolerance to nonsteroidal anti-inflammatory drugs;
      • requirement for antibiotic prophylaxis
      • open tooth apex
      • pacemaker use
      This randomized controlled clinical study was conducted to compare the incidence and intensity of post-obturation pain, evaluate the overextension of filling material radiographically, and assess the relationship between pain and analgesic intake in patients with vital and devital teeth undergoing carrier-based obturation with two different sealers (iRoot SP, AH Plus)
      Status:
      completed
      Type:
      Interventional
      Phase:
      -
      Start:
      30 June, 2015
      Updated:
      23 January, 2017
      Participants:
      160
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