A post-operative pain evaluation with Ultrasonic activation and laser irradiation using continuous chelation irrigant solution in symptomatic irreversible pulpitis teeth A Randomized Clinical Study

A comparative evaluation of post-operative pain with Ultrasonic activation and laser irradiation using irrigation of 9 % etidronate & 2.5% NaOCl mixed solution in symptomatic irreversible pulpitis teeth A Randomized Clinical Study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067190

Enrollment

Registered

2024-05-10

Start date

Unknown

Completion date

Unknown

Last updated

2025-03-03

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Ultrasonic activation: irrgation solution will be activated with the help of ultrasonic activator for 1min. Control Intervention1: 980nm Diode laser: after irrigation protocol root can

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy patients (Category: American Society of Anaesthesiologists class 1) (ASA House of Delegates 2014) aged between 18 – 60 years of age will be included. 2. maxillary or mandibular teeth diagnosed with Symptomatic irreversible pulpitis with or without periapical pathology or radiographic rarefaction. 3. Only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Teeth with open apex, root resorption and calcified pulp chamber and canals will be excluded from the study. 2. Teeth with curvature more than 20 degree will be excluded from the study 3. patients taking analgesics 12 hours before the intervention. 4. Teeth which had received previous endodontic treatment will be excluded from the study. 5. Cases showing periodontal pockets deeper than 4mm will be excluded from the study. 6. Teeth with pre-op swelling, draining sinus and Flare ups during root canal treatment will be excluded from the study. 7. Any other iatrogenically affected root canal treatments will be excluded from the study. 8. Medically compromised patients will be excluded from the study.

Design outcomes

Primary

Measure	Time frame
The result of this study will help us to know about postoperative comfort of patient after ultrasonic activation and 980nm diode laser disinfection with continous chelation protocol.Timepoint: preoperative pain score and postoperative at 6, 12, 24 and 48 hours	—

Secondary

Measure	Time frame
To know which has better efficacy than the other.Timepoint: at post operatively 6hrs, 12hrs, 24hrs, 48 hrs	—

Countries

India

Contacts

Public ContactVinaya pisal

KM Shah Dental College and Hospital Sumandeep Vidyapeeth

drrenubatra@gmail.com9607086688

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026