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Grape Seed Extract VS Low Level Laser Therapy for Dentin Hypersensitivity

Comparison of the Effectiveness of Grape Seed Extract (GSE) and Low-level Laser Therapy in the Management of Dentin Hypersensitivity: A Randomized Control Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05927831
Enrollment
30
Registered
2023-07-03
Start date
2023-05-15
Completion date
2024-01-15
Last updated
2023-07-03

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

Conditions

Dentin Hypersensitivity

Brief summary

Dentin hypersensitivity (DH) is a common clinical problem frequently seen in dental patients. According to Splieth et al., the prevalence of dentin hypersensitivity is 3-98% in adult population.DH is described as a short, sharp pain or discomfort that responses to certain stimuli, typically thermal, tactile, osmotic or chemical, due to exposed dentinal surface which can be explained by the hydrodynamic theory. The laser is a narrow, focused beam of light emitted to vaporise, fuse, melt, or seal dentinal tubules using laser heat to induce hydroxyapatite crystals for recrystallisation of the mineral component of dentine. The obliteration of dentinal tubules is caused by heat generated by laser beam which inhibits the transmission of the stimulus in the dentinal tubules. Grape seed extract contains proanthocyanidins (PA) which is able to bind to proline-rich proteins, like collagen, and contributes in enzyme proline hydroxylase activity that is essential for the biosynthesis of collagen in the dentin. The cross-linking action of collagen fibrils in dentin also able to prevent mineral loss.

Interventions

Grape seed extract will be applied in the form of a gel on the tooth surface

DEVICELow-level laser therapy

The device will be set at a wavelength of 810 nm, with a power output of 0.5 watts tip of diameter 300 μ in non-contact mode

Sponsors

Manipal University College Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with at least three sensitive tooth by gingival recession or tooth wear \>2 scores on the VAS scale. * Tooth wear index score \<3 (Smith and Knight tooth wear index) * Systemically healthy patient. * 20-50 years of age.

Exclusion criteria

* Teeth with caries, cracked teeth, mobile teeth and pulpitis. * Deep periodontal pockets (probing depth \>6 mm), periodontal surgery within the previous 3 months. * Recent desensitizing therapy * systemic diseases and gastric diseases (GERD) * Allergy to active ingredients.

Design outcomes

Primary

MeasureTime frameDescription
The patients' dentin hypersensitivity levels will be measured using a visual analogue scale (VAS)1st dayThe patients' dentin hypersensitivity levels will be measured using a visual analogue scale (VAS)(0 to 10) before and after treatment.

Countries

Malaysia

Contacts

Primary ContactAnchu R Thomas
rachel.thomas@manipal.edu.my+601127292297

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026