A clinical trial to study the effect of Gluma and Er,Cr:YSGG Laser in patients with tooth hypersensitivity

Comparative assessment on effect in hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin after pre-treatment with Gluma and Er,Cr:YSGG Laser VS without pre-treatment : A Randomized Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064425

Enrollment

Registered

2024-03-19

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

None listed

Interventions

Intervention1: Gluma: after pretreatment with Gluma, non-carious lesion restored with adhesive resin. Intervention2: Er,Cr:YSGG laser: after pretreatment with laser, non-carious lesion restored with a

Eligibility

Inclusion criteria

Inclusion criteria: Premolar with Class 3 Non-Carious Cervical Lesion showing hypersensitivity. Patient showing willingness to participate in the study for 1 month.

Exclusion criteria

Exclusion criteria: i. Carious lesion on the selected or neighbouring tooth. ii. Restorations on the selected tooth. iii. Any desensitizing therapy on the selected tooth during the last 6 months iv. Periodontal surgery within last 3 months v. Nonvital tooth, cracked tooth syndrome vi. Tender tooth in the same quadrant as the hypersensitive teeth. vii. Patients undergoing orthodontic treatment viii. Pregnant/lactating females. ix. Smokers, alcoholics. x. Patients taking antibiotics/analgesics/anti-inflammatory/anti-depressive drugs, patients having cognitive dysfunctions/general communication difficulties.

Design outcomes

Primary

Measure	Time frame
1)To assess the hypersensitivity in Non-Carious Cervical Lesions (NCCLs). 2)To assess the effect in hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin after pre-treatment with Gluma and Er,Cr:YSGG laser vs without pre-treatment. 3)To compare the efficacy of Gluma and Er,Cr:YSGG laser in reducing hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin vs without pre-treatment. Timepoint: VAS scale will be used to measure the pain response before treatment 24hrs post restoration 15 days and 1 month.	—

Measure

Time frame

1)To assess the hypersensitivity in Non-Carious Cervical Lesions (NCCLs). 2)To assess the effect in hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin after pre-treatment with Gluma and Er,Cr:YSGG laser vs without pre-treatment. 3)To compare the efficacy of Gluma and Er,Cr:YSGG laser in reducing hypersensitivity in Non-Carious Cervical Lesions (NCCLs) restored with adhesive resin vs without pre-treatment. Timepoint: VAS scale will be used to measure the pain response before treatment 24hrs post restoration 15 days and 1 month.

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Secondary

Measure	Time frame
no secondary outcomeTimepoint: nil	—

Countries

India

Contacts

Public ContactDr Sagarika Sortey

Department Of Conservative Dentistry and Endodontics, VSPM DC RC

badole_g15@yahoo.co.in9665410655

Outcome results