Status:
COMPLETED
Evaluation of Air Polishing With Ultrasonic Debridement in the Treatment of Initial Periodontal Pockets
Lead Sponsor:
Syrian Private University
Conditions:
Gingivitis
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
Clinical evaluation of using erythritol powder as air polishing with ultrasonic scaling and root planing in the treatment of initial periodontal pockets. This trial will be split-mouth design, in whic...
Detailed Description
The aim of the study is to evaluate the usage of erythritol powder by means of air polishing in hand of undergraduate dental students as a single way to remove biofilm and the adjunctive application o...
Eligibility Criteria
Inclusion
- Patients are in generally good health
- Patients are from both gender and their age is between 18 to 60 years.
- Patients have a minimum of 20 teeth
- The patient is a non-smoker (less than 5 cigarettes per day) and non-alcoholic.
- Female participants must not be pregnant or breastfeeding (lactation).
- the absence of severe oral habits
- the presence of at least one residual pocket with pocket depth \>4 mm with interdental sites with a probing depth of 3 to 5 mm without furcation involvement or subgingival restorations.
- A sign informed consent from participation and permission to use obtained data for research purposes.
Exclusion
- Bruxism
- Allergy to glycine or chlorhexidine;
- systemic medical conditions requiring antibiotic prophylaxis (for endocarditis prophylaxis) and anti-inflammatory drugs before dental procedures;
- active systemic infectious disease;
- major systemic illnesses (diabetes mellitus, cancer, immunodeficiency virus, bone metabolic diseases or disorders that compromise wound healing, radiation or immunosuppressive therapy, neutropenia, agranulocytosis, or bleeding disorders.
- chronic high dose steroid therapy
- Patients are undergone to radiotherapy or chemotherapy before or during the study period.
- actively smoking more than five cigarettes per day;
- signs of generalized severe periodontitis;
- having received periodontal maintenance within 3 months before baseline
- patients treated with antibiotics 6 months prior to the study
- chronic bronchitis and asthma
- compromised immune system
- hypersensitivity to sugar alcohols.
- any physical limitations or restrictions that might preclude normal oral hygiene procedures.
Key Trial Info
Start Date :
February 9 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 30 2019
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT03863093
Start Date
February 9 2019
End Date
December 30 2019
Last Update
November 24 2023
Active Locations (1)
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1
Syrian Private University
Damascus, Syria