Assessment of the Efficacy of Root Canal Treatment Utilizing PLAZEN RCT: A Clinical Study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0009611

Enrollment

Registered

2024-07-09

Start date

2024-07-03

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Medical Device : 1) Test group: Cases where root canal treatment was performed using PLAZEN RCT 2) Control group: When root canal treatment was performed using sodium hypochlorite solution * Assessme

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Those with clinical symptoms (pain, gingival swelling, gingival abscess, etc.) due to periapical lesions 2) Those who agree to participate in clinical trials and sign the subject consent form

Exclusion criteria

Exclusion criteria: 1) Those who have received cochlear implant or pacemaker procedures 2) Those whose pain is not odontogenic 3) Diabetic patients, immunocompromised patients, pregnant women 4) Periodontally damaged teeth, teeth not suitable for rubber dam isolation 5) When participation in a clinical trial is judged to be inappropriate because it may affect other ethical or clinical trial results.

Design outcomes

Primary

Measure	Time frame
Assess changes in periapical radiolucency	—

Secondary

Measure	Time frame
VAS/tooth movement/percussion response	—

Countries

Korea, Republic of

Contacts

Public ContactLim eun ji

Hallym University Medical Center

eunjiiiii_@naver.com+82-31-380-1513

Outcome results