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Evaluating the Wavelengths of Laser for managing pain after single sitting Root Canal treatment

Comparative Evaluation Of Photobiomodulatory Effect Of 660nm and 970nm Diode Laser On PostOperative Pain Management In Single Visit Endodontic Treatment A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080023
Enrollment
84
Registered
2025-02-07
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: K040- Pulpitis

Interventions

Intervention1: Photobiomodulation with 660nm Wavelength Diode Laser: Post operative pain evaluation after Root canal treatment using Photobiomodulation therapy with 660nm laser at 100mW Power exposur

Sponsors

PRIYANKAR ROY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients requiring root canal treatment of maxillary 1st premolar teeth with two root canals, diagnosed clinically as asymptomatic irreversible pulpitis using pulp sensitivity tests. 2.Patients ranging in the age group of 18-50 years. 3.Patients with non-contributory medical history. 4.Teeth with adequate coronal structure to ascertain proper isolation.

Exclusion criteria

Exclusion criteria: PATIENT-SPECIFIC: 1.Patients who refuse to consent to the procedure. 2.Patients with any systemic diseases, pregnancy, or immunocompromised conditions. 3.Patients on any antibiotic therapy in the past 3 months 4.Patients on any analgesic drugs in the past 7 days 5.Patients allergic to lignocaine in 1:1,00,000 concentration adrenaline 6.Patients requiring root canal treatment of two or more teeth ipsilaterally (since the pain caused by any of these teeth can result in false positive reading) B. SPECIFIC TO DIAGNOSIS: 1.Teeth with acute apical periodontitis 2.Teeth with acute periapical abscess 3.Teeth with an inflammatory exudate draining through the canal. 4.Necrotic painful teeth with absence of sinus tract for drainage 5.Re-treatment cases 6.Anatomically complicated tooth 7.Teeth with aggressive periodontitis or grade III mobility

Design outcomes

Primary

MeasureTime frame
To assess and conduct an intragroup and intergroup comparison of the intensity & incidence of post-operative pain at 6, 24, 48 and 72 hours using Visual analog scale without performing photo-biomodulation,with performing photobiomodulation with 660nm and 970nm wavelengthsTimepoint: 6, 24, 48 and 72 hours—

Secondary

MeasureTime frame
To evaluate & compare the association of variables (age & sex) between groupsTimepoint: 6 24 48 & 72 hours—

Countries

India

Contacts

Public ContactDr Sonal B Joshi

KAHER KLE Vishwanath Katti Institute Of Dental Sciences

roypriyankar09@gmail.com7975161191

Outcome results

None listed

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