Cryotherapy on Inflammatory Profile and Postoperative Pain Levels in Endodontic Infections

NCT04798144 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2022-06-10

No results posted yet for this study

Summary

The aim of this study is to evaluate the effects of cryotherapy applications on the inflammatory cytokine and collagenase matrix metalloproteinase levels during root canal treatment and postoperative pain intensity and incidence. Mandibular premolar teeth of 60 male patients within the 20-30 years old range, diagnosed with asymptomatic apical periodontitis will be included to the study for this purpose. The experimental protocols consist clinical and laboratory phases. In clinical phase, procedures of cryotherapy and control groups will be applied in 2-visit-root canal treatment. The samples, which were collected during root canal treatment, will be subjected to enzyme-linked immunosorbent assay (ELISA) analysis in laboratory. Levels of interleukin and inflammatory destructive enzymes will be determined in collected samples. During the analysis of visual analogue scale scores, the correlation between the changes of the cytokine and proteolytic enzyme levels and presence and intensity of pain will be evaluated.

Conditions

  • Apical Periodontitis
  • Postoperative Pain
  • Cytokine Levels

Interventions

DEVICE

Distilled water irrigation kept at 2.5°C degree

The use of cold distilled water for final irrigation of root canal system during root canal treatment

DEVICE

Distilled water irrigation kept at room temperature

The use of distilled water kept at room temperature for final irrigation of root canal system during root canal treatment

Sponsors & Collaborators

  • The Scientific and Technological Research Council of Turkey

    collaborator OTHER
  • Ondokuz Mayıs University

    lead OTHER

Principal Investigators

  • Elif Kalyoncuoğlu, PhD · Ondokuz Mayıs University

  • Abdurrahman Aksoy, PhD · Ondokuz Mayıs University

  • Ayşegül Arkan, DDS · Ondokuz Mayıs University

  • Onur Kömeç, DDS · Ondokuz Mayıs University

  • Elçin Yüzgüleç, DDS · Ondokuz Mayıs University

  • Hande Akgün, DDS · Ondokuz Mayıs University

  • Sabiha G Afak, DDS · Ondokuz Mayıs University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
30 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-11-15
Primary Completion
2022-03-31
Completion
2022-04-15

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04798144 on ClinicalTrials.gov