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Clinical Trials/NCT03029520
NCT03029520CompletedNot Applicable

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

Cukurova University0 sites160 target enrollmentStarted: July 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ayfer Atav Ateş

Research assistant

Cukurova University

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