Casein Phosphopeptide and Diode Laser in Treating Dentin Hypersensitivity: A Clinical Study.
Sanam Faheem, Rimsha Qasim, Chander Kumar...
https://pubmed.ncbi.nlm.nih.gov/41789288Actively Recruiting
Phase Not Applicable
Age: 25Years - 65Years
All Genders
Healthy Volunteers
ID06463938
A Clinical Study to Evaluate the Effectiveness of Casein Phosphopeptide Amorphous Calcium Phosphate Paste Alone or with Lasotronix Diode Laser to Treat Dentin Hypersensitivity
Led by Dow University of Health Sciences · Updated on 2024-07-26
120
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Dentin hypersensitivity (DH) causes sharp, short pain from exposed dentin triggered by chemicals, temperature, or touch. It commonly affects older adults and varies widely in prevalence. This research evaluates the effectiveness of Casein phosphopeptide paste (CPP-ACP) alone or combined with a diode laser called Lasotronix in treating DH, as limited studies have explored this combination. The study involves four groups: one receiving CPP-ACP paste application only, one receiving diode laser therapy only, a third receiving both CPP-ACP and laser treatments, and a control group with no treatment. Lasotronix uses a 635nm wavelength laser designed for safe and effective bio-stimulation and photo-disinfection, while CPP-ACP paste aims to reduce pain by managing dentin sensitivity. Participants aged 25 to 65 with at least one sensitive, vital tooth without decay or defective restoration will be involved. They will undergo treatment and follow-up to assess dentin hypersensitivity over three months. Researchers will monitor pain levels and treatment effects, ensuring safety and adherence to the study protocol throughout the trial period.
CONDITIONS
Brief Title
A Clinical Trial to Compare Lasotronix Alone or in Combination With CPP-ACP to Treat DH
Who Can Participate
Age: 25Years - 65Years
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
- Patients of any gender aged 25 to 65 years
- Must have at least one sensitive and vital tooth without decay or defective restoration
You will not qualify if you...
- History of desensitizing therapy on the affected tooth in the last six months
- Use of antibiotics, analgesics, or anti-inflammatory drugs
- History of smoking
- Pregnancy
- Not willing to participate or attend follow-ups
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Treatment
Duration - Up to 3 months
Participants receive one of the following: CPP-ACP paste application, diode laser therapy, or a combination of both to treat dentin hypersensitivity.
Trial Site Locations
Total: 1 location
1
Dr Sanam Faheem
Karachi, Sindh, Pakistan, 75330
Actively Recruiting
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Research Team
S
Sanam Dr Faheem, MSc
C
Chandar Dr Kumar
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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