Effect of Cryotherapy and Laser Application on Post-Operative Pain in Single Visit Endodontically Treated Symptomatic Apical Periodontitis Cases

NCT06657664 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-10-24

No results posted yet for this study

Summary

This study compare the effect of applying ice after single visit endodontic treatment with lasers to reduce post operative pain .

Conditions

  • Irriversible Pulpitis With Apical Peridontitis
  • Hot Tooth

Interventions

PROCEDURE

cryotherapy with sterile saline at 2.5ºC

the root canals are given a final irrigation with 20 mL cold (2.5oC) saline solution for 5 minutes before obturation

PROCEDURE

intaoral cryotherapy

ice sticks (wrapped in sterile gauze if needed) using plastic pipette droppers filled with freezed sterile water are placed intraorally in the mouth on the apices of the treated tooth on both buccal and palatal sides for 30 minutes

PROCEDURE

Both intracanal and intraoral cryotherapy

Canal is irrigated with iced saline for 5 minutes before obturation . Root canal is obturated and coronal restoration is done. Then, application of intraoral cryotherapy is performed by ice sticks for 30 minutes.

DEVICE

Low Level Laser Therapy

laser irradiation on the soft tissues covering the apices of the tooth on both buccal and palatal surfaces respectively

PROCEDURE

Control (Standard treatment)

, all occlusal contacts were reduced by 1 mm

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2024-09-01
Completion
2024-10-10
FDA Device
Yes

Countries

  • Egypt

Study Locations

More Related Trials

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 NCT06657664 on ClinicalTrials.gov