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Comparative evaluation of diode laser and seventh generation dentin bonding agent in the treatment of dentinal hypersensitivity

Dentin cryesthesia - Evaluating the efficacy of diode laser and seventh generation bonding agent : A clinical study - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067589
Enrollment
20
Registered
2024-05-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: K031- Abrasion of teeth

Interventions

Intervention1: DIODE LASER: BIOLASE EPICX WITH TTP (E4-4 EZ) WITH SPECIFICATIONS OF 2W POWER,980nm,KEEPING THE TIP 2mm AWAY FROM THE TOOTH WITH CONTINUOUS MODE FOR 30sec AND MOVING THE TIP ALL OVER TH

Sponsors

Khushi Patel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with good general health with no allergies to commercial dental products No use of desensitizing toothpaste within prior 3 months No restoration or decay of tested teeth Hypersensitivity due to etiologies like abrasion, parafunctional habits, gastric or emotional diseases or frequent ingestion of acidic foods Gingival recession of Miller class 1 and 2

Exclusion criteria

Exclusion criteria: Non vital teeth or vital teeth with cracks, restorations, carious lesions Occlusal facets Use of any desensitizing toothpaste within last 3 months Teeth with periapical pathology Patients with chronic disease with daily pain episodes, those under anticonvulsive, analgesic, antihistaminic, tranquillizer, anti inflammatory or sedative medication in last 72 hours Prior periodontal surgery in last 6 months Fixed partial units and prosthetic clasp Pregnant and nursing females

Design outcomes

Primary

MeasureTime frame
Respond to air blow and tactile stimulusTimepoint: Immediate postoperative, 7 days, 14 days, 1 month, 3 months, 6 months

Secondary

MeasureTime frame
Having any complication of severe sensitivity within follow up period time, all the measures were recorded in patients chartsTimepoint: Immediate postoperative, 7 days, 14 days, 1 month, 3 months, 6 months

Countries

India

Contacts

Public ContactKhushi Patel

College of Dental Sciences and Research Centre

drshah16@gmail.com9376121229

Outcome results

None listed

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