Clinical Trial: Post-Obturation Pain Following the Use of the AH Plus and iRoot SP Sealers

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: Termoplastik Kor tekniğini Iki farklı Kanal patı Ile kullanıp Tedavi sonrası Hassasiyet ve kök Ucundan taşma miktarının değerlendirilmesi: Randomize k

Brief Summary:

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..

Detailed Summary: 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)
Sponsor: Cukurova University

Current Primary Outcome: The incidence of postoperative pain by using VAS scale after obturation with different sealers. [ Time Frame: 72 hour ]

Original Primary Outcome: To assess The incidence of postoperative pain by using VAS scale after obturation with different sealers. [ Time Frame: 72 hour ]

Current Secondary Outcome:

Original Secondary Outcome:

Information By: Cukurova University

Dates:
Date Received: January 11, 2017
Date Started: July 2015
Date Completion:
Last Updated: January 24, 2017
Last Verified: January 2017