Postoperative Pain After the Use of Different Last Irrigation Method During Root Canal Treatment in Primary Teeth
NCT ID: NCT04197531
Last Updated: 2019-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
110 participants
INTERVENTIONAL
2018-04-01
2019-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
EndoActivator
Irrigation Method
Irrigation Method
Conventional Endodontic Syringe
Irrigation Method
Irrigation Method
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Irrigation Method
Irrigation Method
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* American Society of Anesthesiologists class 1 patients aged 5-9 years
* Patients with symptomatic irreversible pulpitis of maxillary primary molars confirmed using periapical radiographs, percussion, and cold test
* Patients having teeth with two-thirds of each root remaining
* Absence of periapical lesions and interradicular radiolucency
* Moderate to very severe (2-4) five-face scale pain scores in the 24-hour period before the procedure.
Exclusion Criteria
* Teeth with pathologic root resorption
* Teeth with excessive mobility.
5 Years
9 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
TC Erciyes University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Husniye Gumus
Study Director, PHD., Dr.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hüsniye Gümüş, PHD., Dr.
Role: STUDY_DIRECTOR
Erciyes University, Faculty of Dentistry
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Erciyes University, Faculty of Dentistry
Kayseri, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Ramamoorthi S, Nivedhitha MS, Divyanand MJ. Comparative evaluation of postoperative pain after using endodontic needle and EndoActivator during root canal irrigation: A randomised controlled trial. Aust Endod J. 2015 Aug;41(2):78-87. doi: 10.1111/aej.12076. Epub 2014 Sep 4.
Yilmaz K, Tufenkci P, Adiguzel M. The effects of QMix and EndoActivator on postoperative pain in mandibular molars with nonvital pulps: a randomized clinical trial. Clin Oral Investig. 2019 Nov;23(11):4173-4180. doi: 10.1007/s00784-019-02856-6. Epub 2019 Feb 27.
Gumus H, Delikan E. The effect of sonic activation of irrigant on postoperative pain after root canal treatment in primary molar teeth: a randomized, clinical study. Clin Oral Investig. 2021 Jan;25(1):363-370. doi: 10.1007/s00784-020-03687-6. Epub 2020 Nov 12.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2018/152
Identifier Type: -
Identifier Source: org_study_id