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Evalution the effect of nanobioglass and diode laser (980 nm) in dentin hypersensitivity treatment

Evaluation the effect of nano bioglass and diode laser (980 nm) in dentin hypersensitivity treatment: a 6-month clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240109060667N1
Enrollment
15
Registered
2024-02-05
Start date
2024-01-10
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

dentin hypersensivity. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: Control group: No laser or nanobio-glass were applied on dentin surfaces. Intervention 2: NB group (Nanobioglus): 50% solution of biogas nanoparticles and distilled water was prepared.

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Good general health No known allergy to commercial dental products Teeth studied have no decay or repair The patient has not previously received treatment for their dentinal allergy. The patient should be able to determine the pain score in VAS in terms of age and mentality. Patients should not have a history of receiving bleaching treatments by bleaching method.

Exclusion criteria

Exclusion criteria: People with chronic diseases with episodes of daily pain who have taken anticonvulsants? analgesics ? antihistamines ? sedatives ? anti-inflammatory or analgesic drugs in the past 72 hours. People who have used toothpaste or hypoallergenic mouthwashes in the past 3 months. People who have had periodontal surgery in the past 6 months. White bread teeth or white teeth that have cracks, previous repairs, caries lesions or active periodontal disease. Subjects with periodontal recession will remain active in the study. People with deep cavities in the vicinity of sensitive teeth are likely to be mistaken for sensitive tooth pain.

Design outcomes

Primary

MeasureTime frame
People whose VAS scores are above 5. Timepoint: Patients were called for followup after 1 week, 1 month and 6 months after treatment. At each visit, the mentioned evaluation process was repeated for each patient and VAS score was recorded. Method of measurement: The lowest score is zero which means the situation is completely painless, and the highest score is 10, which means the maximum amount of pain that a person can experience.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Khalafi

Hamedan University of Medical Sciences

sahel21975@gmail.com+98 917 758 5429

Outcome results

None listed

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