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Clinical evaluation of the effect of Er:YAG in treating abrasion caused dentin hypersensitivity

Clinical outcomes research of the effect of Er:YAG in treating abrasion caused dentin hypersensitivity: a randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010245
Enrollment
Unknown
Registered
2016-12-24
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Dentine Hypersensitivity

Interventions

control group of Desensitizer:Gluma Desensitizer
experimental group of Er:YAG laser:Er:YAG laser treatment on hypersensitive dentin

Sponsors

Dept. of General Dentistry & Emergency, School of Stomatol, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients must have subjective symptom of Dentine Hypersensitivity caused by abrasion, and the study teeth must be filling free and restoration free; 2. Patients must not have used desensitizing toothpaste within the past 3 months, undergone desensitization treatment with desensitizer within the past 1 year, or undergone the desensitization treatment with laser; 3. There must be no caries, crack or other factors which might impact therapy to the study teeth. No other dental therapy except for desensitization to the study teeth; 4. Patients must be able to read and understand the consent form and be willing to sign it.

Exclusion criteria

Exclusion criteria: 1. Teeth that have be treated with periodontal surgery within the past 6 months or scaling/root planning within the past 3 months; 2. Patients have the contraindications with the laser treatment; 3. Patients are not able to independently or accurately describe their self subjective feeling; 4. Patients suffer from the chronic diseases or pain; 5. patients suffer from the serious physical or mental diseases; 6. Patients have undergone other clinical trial; 7. Patients have the history of drug and alcohol addiction; 8. Patients are currently being treated with drugs which may influence the sensory nerve or the dental disease.

Design outcomes

Primary

MeasureTime frame
visual analog scale;

Countries

China

Contacts

Public ContactChen YongJin

School of Stomatology, Fourth Military Medical University

cyj1229@fmmu.edu.cn+86 13991979822

Outcome results

None listed

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