Skip to content

Effect of Different Irrigation Activating Techniques on Irrigant Penetration Depth and on Post-Operative Pain

Effect of Different Irrigation Activating Techniques on Irrigant Penetration Depth Into Root Canals and on Post-Operative Pain After Single-Visit Endodontic Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05450003
Enrollment
30
Registered
2022-07-08
Start date
2022-08-01
Completion date
2022-11-25
Last updated
2023-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irrigation Activation

Brief summary

Irrigation activation in endodontics is considered now a very important step for the success of root canal treatment. In this study, the investigator will examine the effect of two recent activation systems ( XP-endo Finisher file and the new sonic EDDY system) in comparison with the conventional needle irrigation on irrigant penetration depth into root canals using radiopaque contrast media and digital radiography and on the postoperative pain after single-visit endodontic treatment using a visual analog scale.

Interventions

DEVICEIrrigation activation using xp endo finisher file , new sonic eddy tip and conventional needle syringe irrigation

irrigation activation using 3 different irrigation activation systems including xp endo finisher file , new sonic eddy system and conventional needle syringe irrigation

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

the study will evaluate 3 groups of patients each consists of 10 participants receiving different type of irrigation activation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Asymptomatic vital/non vital teeth requiring root canal treatment. * Teeth with sound periodontal apparatus. * Teeth without pus or inflammatory exudates draining through the canal. * Teeth without anatomic variations. * Teeth with sinus tract. * Teeth without history of trauma. * Patients not on analgesics or sedative medication prior to root canal therapy

Exclusion criteria

* • Patients with any systemic diseases. * Pregnant or lactating patients. * Immunocompromised patients. * Apparently thin roots in which apical preparation with #40 file would be overzealous. * Patient allergic to anything used in this procedure especially rubber dam material and Iohexol (radiographic contrast media). * Teeth with calcified canals. * Patients with acute apical periodontitis, acute apical abscess, and weeping canals. * Necrotic painful teeth with the absence of sinus tract for drainage.

Design outcomes

Primary

MeasureTime frameDescription
irrigant penetration depththrough study completion, an average of 3 monthsmeasurement of irrigant penetration depth using radioaque media and digital radiography
postoperative painthrough study completion, an average of 3 monthsevaluation of postoperative pain using visual analog scale VAS with scores from 0 to 100. score 0 indicated no pain while score 100 indicates maximum pain

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026