Postoperative Pain After İntracanal Procedures

Endodontically Treated Teeth Clinical Trial

Official title:

Postoperative Pain After İntracanal Procedures Based On Different İrrigation Activation Tecniques: A Randomized, Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04892355
• Other study ID #: AfyonkarahisarHSU
• Status: Not yet recruiting
• Phase: N/A
• Start date: August 6, 2022
• Est. completion date: November 6, 2022

Study information

• Verified date: February 2022
• Source: Afyonkarahisar Health Sciences University
• Contact: yahya güven
• Phone: 05314599583
• Email: yahyaguven52[@]outlook.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aim: The aim of this study is to investigate the effects of different irrigation activation systems on pain after endodontic treatment in molar teeth with irreversible pulpitis.Post-operative pain values of the participants will be recorded and evaluated with the VAS scale. Postoperative pain values of the techniques will be compared with statistical evaluation.

Description:

Aim: The aim of this study is to investigate the effects of different irrigation activation systems on pain after endodontic treatment in molar teeth with irreversible pulpitis.Materials and Methods: The study will be carried out on 140 patients with molar teeth diagnosed with irreversible pulpitis. After the root canal preparation is completed, the patients will be divided into 4 groups according to the irrigation activation system; Conventional syringe irrigation (CSI), EDDY, EndoActivator (EA) and Xp-endo Finisher (XPF). After the irrigation process is completed, the root canals will be filled using gutta-percha and canal sealer and the treatment will be completed in one session. Pain values at 6, 24, 48, 72 hours and 7 days after treatment will be evaluated at a 0.05% significance level using the Kruskal-Wallis test.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 140
• Est. completion date: November 6, 2022
• Est. primary completion date: October 6, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Healthy patients ranging between 18 and 60 years in age
• Patients that experienced moderate-to-severe pain represented on a visual analogue scale (VAS)
• Maxillar and Mandibular molar teeth were diagnosed with symptomatic irreversible pulpitis

Exclusion Criteria:

• Any systemic disease and pregnancy in the patient
• Having used analgesic-anti-inflammatory in the last 12 hours and cortisone for the last 6 months
• The patient has bruxism
• Teeth with severe damage
• Teeth with calcified canals
• Teeth with pain to percussion
• Teeth with periapical radiolucency
• Teeth with root resorption
• Teeth with an immature / open apex
• Teeth with previous RCT

Related Conditions & MeSH terms

• Endodontically Treated Teeth
• Pain, Postoperative
• Tooth, Nonvital

Intervention

Device:
• Root canal irrigation
Devices used during root canal irrigation

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Afyonkarahisar Health Sciences University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative Pain After Intracanal Procedures Based On Different Irrigation Activation Tecniques: A Randomized, Clinical Trial	Preoperative pain of the patients before the treatment was recorded with the VAS scale. Pain levels were classified as 0: no pain, 1-3: mild pain, 4-6: moderate pain, 7-10: severe pain .After the treatment of the patients, a pain assessment form was given to the patient in order to evaluate the postoperative pain. Patients were asked to mark their pain levels on the VAS scale. The marking procedure was taught to the patients by a blinded researcher from the groups. When the patients came to the control appointment, VAS scales were collected and the data were analyzed.	one week(7 days)