Dentin Sensitivity Clinical Trial
Official title:
Molar Incisor Hypomineralization and Hypersensitivity in Paediatric Age: a Comparison of Treatment Protocols
The aim of this study was to evaluate the efficacy of the association of casein phosphopeptide plus amorphous calcium phosphate (CPP-ACPF) mousse and photo-bio-modulation therapy (PMBT) (diode laser, RAFFAELLO 980 BIO - Dental Medical Technologies - DMT S.r.l.) in the treatment of dental hypersensitivity (DH) in children with Molar Incisor Hypomineralization (MIH) . Children aged 6-14 years with hypersensitive teeth were randomized into 3 groups. Group A received the application of CPP-ACPF mousse (GC MI Paste®) and sham light therapy; group B got the application of placebo mousse (Elmex Junior®) and PMBT; group C received both CPP-ACPF mousse and PMBT.
Status | Recruiting |
Enrollment | 39 |
Est. completion date | May 1, 2023 |
Est. primary completion date | February 10, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 6 Years to 14 Years |
Eligibility | Inclusion Criteria: - children 6-14 years old - having at least one MIH-affected tooth and MIH-associated hypersensitivity. Exclusion Criteria: - allergy to milk proteins - chronic diseases, - carious lesions on the sensitive teeth - restorations on the sensitive teeth - other enamel defects (fluorosis, amelogenesis/dentinogenesis imperfecta…) - presence of orthodontic appliance - recent anti-inflammatory or cortisone therapies - recent desensitizing treatments. |
Country | Name | City | State |
---|---|---|---|
Italy | Dental Clinic | Brescia |
Lead Sponsor | Collaborator |
---|---|
Università degli Studi di Brescia |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Treatment of dental hypersensitivity (DH) | The efficacy of the treatment of dental hypersensitivity was evaluated using the Visual Analogue Scale (VAS), ranging from 0 to 10, with 0=no pain and 10= worst possible pain. The evaluation was performed at the following time points: before (T0) and after (T1) the first session, after the second session (T2) on the 7th day, after the third session (T3) on the 14th day and after 4 weeks from the starting (T4) on the 28th day. | 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02753075 -
A Study in Dentinal Hypersensitivity (DH) Participants to Assess the Efficacy of an Occluding Dentifrice.
|
N/A | |
Completed |
NCT06045026 -
A Real-World Evidence Study Evaluating Oral Health Related Quality Of Life With Use Of A Stannous Fluoride Anti-Sensitivity Toothpaste For Dentin Hypersensitivity Management
|
N/A | |
Completed |
NCT02861664 -
Assessment of the Efficacy of an Experimental Occlusion Technology Dentifrice in Dentinal Hypersensitivity
|
N/A | |
Completed |
NCT02542943 -
Efficacy of Two Experimental Oral Rinses in Providing Long Term Relief From Dentinal Hypersensitivity
|
N/A | |
Completed |
NCT02226562 -
Clinical Study Investigating the Efficacy of a Mouthwash in Providing Long Term Relief From Dentinal Hypersensitivity
|
Phase 2 | |
Completed |
NCT02919202 -
Clinical Trial to Compare the Efficacy of a Fluoride Gel and a Dental Bonding Agent in Treatment of Tooth Sensitivity
|
N/A | |
Not yet recruiting |
NCT04485299 -
Clinical Assessment of Bifluorid 10 vs Varnish Fluoride on The Exposed Hypersensitive Cervical Dentin in Adult Patient
|
Phase 2/Phase 3 | |
Completed |
NCT02931734 -
Assessment of Different Protocols for Cervical Dentin Hypersensitivity Treatment
|
N/A | |
Completed |
NCT02923895 -
To Investigate the Efficacy of an Occluding Dentifrice in Dentinal Hypersensitivity (DH)
|
Phase 4 | |
Withdrawn |
NCT03361774 -
A Clinical Method Development Study to Characterise The Efficacy of a Dentifrice For The Relief Of Dentin Hypersensitivity
|
Phase 2 | |
Completed |
NCT02924350 -
The Efficacy of an Occluding Dentifrice in Providing Relief From Dentinal Hypersensitivity (DH)
|
N/A | |
Completed |
NCT05083052 -
Propolis in Reducing Dentin Hypersensitivity
|
N/A | |
Active, not recruiting |
NCT06150573 -
A Study Assessing the Effects of an Experimental Dentifrice in Maintaining Tooth Color Following Tooth Bleaching
|
N/A | |
Completed |
NCT02937623 -
To Evaluate the Efficacy of an Experimental Dissolvable Strip in Rapidly Relieving Dentinal Hypersensitivity (DH)
|
N/A | |
Completed |
NCT02612064 -
The Efficacy of an Occluding Dentifrice in Providing Relief From Dentinal Hypersensitivity
|
N/A | |
Completed |
NCT02293044 -
A Study to Evaluate the Safety and Efficacy of an Oxalate Strip on Adjacent Teeth With Dentinal Hypersensitivity
|
N/A | |
Completed |
NCT02128633 -
Effectiveness of a Homecare Dentin Hypersensitivity Gel
|
Phase 2/Phase 3 | |
Completed |
NCT03310268 -
A Clinical Study to Evaluate a Stannous Fluoride Toothpaste for the Relief of Dentinal Hypersensitivity
|
N/A | |
Completed |
NCT05750745 -
A Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste for the Relief of Dentine Hypersensitivity in a Chinese Population
|
N/A | |
Not yet recruiting |
NCT06417580 -
Effect of Pregabalin Gel in Controlling Cervical Dentin Hypersensitivity
|
Phase 2 |