Termoplastik Kor tekniğini Iki farklı Kanal patı Ile kullanıp Tedavi sonrası Hassasiyet ve kök Ucundan taşma miktarının değerlendirilmesi: Randomize kontrollü Klinik çalışma
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Cukurova University
- Enrollment
- 160
- Primary Endpoint
- The incidence of postoperative pain by using VAS scale after obturation with different sealers.
Study Overview
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 Description
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)
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
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
Outcomes
Primary Outcomes
The incidence of postoperative pain by using VAS scale after obturation with different sealers.
Time Frame: 72 hour
Secondary Outcomes
No secondary outcomes reported
Investigators
Ayfer Atav Ateş
Research assistant
Cukurova University