Overview
Evaluation of the Efficacy of 0.8% Hyaluronic Acid Gel
Status:
Completed
Completed
Trial end date:
2017-10-02
2017-10-02
Target enrollment:
0
0
Participant gender:
All
All
Summary
assess the clinical and laboratory effects of the local and sub gingival application of a 0.8% hyaluronic acid gel (GENGIGEL®) as an adjunct to scaling and root planning (SRP) in chronic moderate to severe periodontitis patients as indicated by expression of Human Beta Definsin-2 (HBD2) in gingival crevicular fluid (GCF).Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Riyadh Colleges of Dentistry and PharmacyTreatments:
Hyaluronic Acid
Criteria
Inclusion Criteria:- Patients should be systemically healthy with moderate to severe chronic periodontitis
of more than 4 mm probing depth in at least two sites in different quadrants.
- Patient should exhibit no known allergies
- Participants should have the ability to attend the hospital regular intervals.
Exclusion Criteria:
- pregnancy
- nursing
- hypertension
- patient with chronic diseases such as diabetes mellitus or rheumatoid arthritis.
-Participants should not be under antibiotics and\or had receive any periodontal
therapy for the last 6 months.
- Participants should not taking drugs that could affect the state of the gingival
tissues.
- Participants must not be undergoing orthodontic therapy, caries free
- Participants must not be using any other supplemental plaque control measures like
mouthwashes.
- Participants should not have the habit of taking alcohol, smoking or chewing tobacco
and do not suffer from any systemic disease.