Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03068533
Other study ID # Abdallah Hassan
Secondary ID
Status Active, not recruiting
Phase N/A
First received February 22, 2017
Last updated February 13, 2018
Start date January 1, 2018
Est. completion date April 1, 2018

Study information

Verified date February 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dentinal hypersensitivity [DH] is a common condition in daily practice, especially in patients who have abrasion, attrition, gingival recession and erosion of teeth. It can affect individuals in the age range of 20-50 years.In a recent systematic review, it was reported that no gold standard treatment modality for dentin hypersensitivity has been established Thus there is a need to evaluate new formulations in different settings and in different populations and to compare those to commonly used agents seeking better results in pain relief for our patients. Studies showed that dentifrice formulations containing 8% arginine in combination with calcium carbonate and fluoride have the ability to plug dentinal tubules, by clumping of both arginine and calcium carbonate that bind with the negatively charged dentin . Aim of the study is to clinically evaluate toothpaste containing 8% arginine, calcium carbonate, and sodium mono-fluorophosphate, in comparison to toothpaste, containing 8% strontium acetate and NaF on the relief of DH in chronic periodontitis patients.


Description:

1. Each eligible patient will be given a number.

2. All eligible patients will receive mechanical debridement in 1 or 2 sessions within 1 week before final evaluation.

3. The hypersensitive teeth will be isolated with cotton rolls, and stimuli will be applied to each tooth for final evaluation after scaling and debridement.

4. Air Sensitivity scale is used to assess sensitivity to air blast, while cold water test and tactile test will be held and assessed by Visual Analog Scale (VAS) , which score from 0 (no pain) to 10 (intense pain).

5. Patients will be handed a 30ml. white package written on it the previously assigned number to them and instructed to brush twice daily with the assigned toothpaste by a soft-bristled toothbrush for 8 weeks, with several returns to the clinic for re-evaluation and to take the refill of the assigned number of toothpaste.

6. Air blast sensitivity score and VAS will be evaluated again weekly and till the end of the evaluation period.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 46
Est. completion date April 1, 2018
Est. primary completion date March 3, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Slight to moderate chronic periodontitis patients diagnosed according to criteria of (Parameter on chronic periodontitis with slight to moderate loss of periodontal support.

American Academy of Periodontology., 2000) as follows : Probing pocket depths up to 6mm Clinical attachment loss (CAL) up to 4mm Class I (incipient) furcation involvement Radiographic evidence of bone loss.

2. At least 2 teeth presenting hypersensitive areas on facial surfaces of teeth with score 2 or 3 on the air sensitivity scale (Pepelassi et al., 2015)

3. Provision of written informed consent

Exclusion Criteria:

1. Chipped teeth.

2. Defective restorations.

3. Deep dental caries or large restorations showing pulpal response.

4. Ongoing treatment with anti-inflammatory drugs.

5. Ongoing treatment for tooth hypersensitivity.

6. Pregnancy.

7. Uncontrolled metabolic diseases.

8. Psychiatric disorder.

9. Smoking

Study Design


Intervention

Other:
8% L-Arginine/calcium carbonate containing toothpaste
use of 8% L-Arginine/calcium carbonate containing toothpaste to relieve hypersensitivity
use of strontium acetate toothpaste
use of strontium acetate toothpaste to relieve hypersensitivity

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary change from baseline Pain (sensetivity) at 8 weeks This will be assessed using VAS that will be determined immediately before product use and then after 8 weeks of daily brushing with the test and control toothpastes following stimulus application using Visual Analog Scale (VAS) baseline and after 8 weeks
Secondary Probing pocket depth probing depth from gingival margin and till base of the pocket or sulcus in mm. baseline and after 8 weeks
Secondary Gingival recession (GR) if present, distance between gingival margin to cemento-enamel junction in mm. baseline and after 8 weeks
See also
  Status Clinical Trial Phase
Completed NCT04249336 - Clinical Efficacy Of BioMin F, Colgate Sensitive Pro-Relief And Sensodyne Rapid Action Dentifrices In DH Phase 3
Completed NCT00763269 - The Efficacy of a Toothpaste to Reduce Sensitivity Phase 3
Recruiting NCT06154941 - Clinical Evaluation of Giomer Based Varnish Versus CPP-ACP Varnish in the Management of Dentin Hypersensitivity: a Randomized Clinical Trial N/A
Completed NCT05501691 - Effect of Diode Laser on Sensitive NCCLs Prior to Composite Restoration N/A
Not yet recruiting NCT04484844 - Clinical Evaluation of Efficacy of Shield Force Plus Varnish VS Sodium Fluoride on Dentin Hypersensitivity Phase 2/Phase 3
Completed NCT02936830 - Effectiveness of Nanohydroxyapetite Paste on Reducing Dentin Hypersensitivity Phase 4
Completed NCT02931734 - Assessment of Different Protocols for Cervical Dentin Hypersensitivity Treatment N/A
Completed NCT04512625 - Desensitizers in Reducing Post Tooth Preparation Sensitivity for a Fixed Dental Prosthesis N/A
Completed NCT05623761 - Toothpastes With Thermal Water for Oral Health Phase 4
Not yet recruiting NCT04731766 - Effect of Using Different Varnishes on Dentin Hypersensitivity; Na Fluoride and Nano-silver Fluoride N/A
Recruiting NCT05927831 - Grape Seed Extract VS Low Level Laser Therapy for Dentin Hypersensitivity N/A
Completed NCT03943095 - Study to Characterize the Efficacy of a Dual Active Dentifrice for the Relief of Dentin Hypersensitivity Phase 2
Not yet recruiting NCT06276777 - The Effect of Using Desensitizers Containing S-PRG In Treatment Of Dentin Hypersensitivity Over 6 Months: A Randomized Clinical Trial N/A
Completed NCT04225247 - Efficacy of Seventh Generation Bonding Agents as Short-Term Desensitizers Among Patients With Hypersensitivity Phase 3
Completed NCT04887181 - The Effects of Different Dentin Hypersensitivity Treatment Methods on Quality of Life N/A
Not yet recruiting NCT03061383 - Reduction of Dentine Hypersensitivity Using 8% Arginine Based Toothpaste and 8% Strontium Acetate Based Toothpaste (DH) N/A
Recruiting NCT03076944 - Evaluation of Desensitization Protocols in Reduction of Dentin Hypersensitivity N/A
Recruiting NCT06264453 - A Study to Evaluate the Efficacy and Safety of KH001 in Patients With Dentin Hypersensitivity Phase 2
Recruiting NCT03083496 - Clinical Evaluation of Different Potassium Oxalate Concentrations in Dentin Hypersensitivity Treatment N/A
Completed NCT03965039 - A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity N/A