Effect of Quercetin in Treatment of Periodontitis

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05928546
Collaborator
(none)
20
2
4

Study Details

Study Description

Brief Summary

Periodontitis is an immune-inflammatory disease affecting the supporting structures of the teeth. It is a disease of multifactorial etiology, with microbial, genetic, environmental and host factors involved, with the release of oxygen-free radicals by the inflammatory cells. Quercetin, have shown potential antimicrobial activity, lowering of inflammatory markers, cholesterol reduction and inhibiting bone loss. However, this data has largely been obtained from in vitro and animal studies, but data from human studies are limited.

Condition or Disease Intervention/Treatment Phase
Phase 1

Detailed Description

Quercetin has been found to decrease the extracellular matrix degradation, promote wound healing when tested in gingival fibroblasts, and showed excellent antibacterial properties. It also possesses antioxidant effect which can be explored to restrict the inflammation in periodontitis. Despite the beneficial effects of Quercetin, its poor aqueous solubility and poor bioavailability result in limited absorption, so scientists have worked on improving the bioavailability of Quercetin using various approaches, such as nanosuspension , self-nano emulsifying systems , microemulsion , solid lipid nanoparticles and cyclodextrin complexes. The combination of oils and emulsifiers enhances the absorption of Quercetin. Hence, nanoemulsion could be a suitable drug delivery vehicle for the loading of Quercetin. Nanoemulsions are more beneficial than microemulsions, as they have high kinetic stability and a smaller droplet size. Therefore, the present study will investigate the efficacy of nanoemulgel of quercetin as adjunct to conventional therapy in treatment of periodontitis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Group(I): 10 sites will receive non-surgical periodontal therapy (scaling and root planing) . Group(Ⅱ): 10 sites will receive non-surgical periodontal therapy followed by the application of quercetin nanoemulgel local delivery 2 times one at the day of non-surgical periodontal therapy and after 2 weeks.Group(I): 10 sites will receive non-surgical periodontal therapy (scaling and root planing) . Group(Ⅱ): 10 sites will receive non-surgical periodontal therapy followed by the application of quercetin nanoemulgel local delivery 2 times one at the day of non-surgical periodontal therapy and after 2 weeks.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Quercetin Nanoemulgel as Adjunct Local Delivery Drug in Non-surgical Treatment of Periodontitis
Anticipated Study Start Date :
Jun 20, 2023
Anticipated Primary Completion Date :
Sep 20, 2023
Anticipated Study Completion Date :
Oct 20, 2023

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Group(I):scaling and root planing only

10 sites will receive non-surgical periodontal therapy (scaling and root planing) .

Device: scaling and root planing
- Full-mouth scaling and root planing was performed in 1-2 sessions within 2 weeks using manual scalers and curettes or ultrasonic scaler and local anesthesia was used in case of need for patient comfort.

Active Comparator: Group(Ⅱ):scaling and root planing with application of quercetin nanoemulgel

10 sites will receive non-surgical periodontal therapy followed by the application of quercetin nanoemulgel local delivery 2 times one at the day of non-surgical periodontal therapy and after 2 weeks.

Drug: Quercetin
Intra-pocket application of quercetin nanoemulgel : After conventional periodontal treatment, the teeth were isolated by cotton rolls for intra pocket application of the gel. That gel was injected in periodontal pocket using syringe with blunt cannula till the gel excess exit from the pocket .

Device: scaling and root planing
- Full-mouth scaling and root planing was performed in 1-2 sessions within 2 weeks using manual scalers and curettes or ultrasonic scaler and local anesthesia was used in case of need for patient comfort.

Outcome Measures

Primary Outcome Measures

  1. Evaluation of the changes in the clinical attachment loss [at base line, 1 month and 3 months after treatment]

    Attachment level was measured using UNC15(University of North Carolina) periodontal probe. Clinical attachment loss was measured as the distance from the cemento-enamel junction to the base of the pocket.

  2. Probing depth [at base line, 1 month and 3 months after treatment]

    The measurement were recorded by UNC15(University of North Carolina) periodontal probe . Pocket depth was measured as the distances from the free gingival margin to the base of the periodontal pocket.

  3. interferon IFN-γ analysis [at base line, 1 month and 3 months after treatment]

    The samples were assayed for (IFN-γ) levels using commercially available enzyme-linked immune-sorbent assay (ELISA) . Highly sensitive ELISA kit was used to detect the (IFN-γ) level in pg/ml in the sample of GCF according to the manufacturer's instructions.

  4. reactive oxygen species (ROS) [at base line, 1 month and 3 months after treatment]

    The samples were assayed for antioxidant effect of quercetin using commercially available reactive oxygen species( ROS) kit . Highly sensitive ROS kit was used according to the manufacturer's instruction

Secondary Outcome Measures

  1. Plaque index (PI) [at base line, 1 month and 3 months after treatment]

    It used to assess plaque accumulation around gingival margin. The degree of plaque accumulation was recorded as follow: 0= No plaque around the gingival margin. 1= A thin film of plaque around the gingival margin. The plaque may be recognized only by running a probe across the tooth surface. 2= Moderate accumulation of soft deposits on the gingival margin and/or adjacent tooth surface, which can be seen by naked eye. 3= Abundance plaque accumulation within the gingival pocket and/or on the gingival margin and adjacent tooth surface and hard deposits on the tooth surface are seen.

  2. Gingival index (GI) [at base line, 1 month and 3 months after treatment]

    It used to assess gingival inflammation. The degree of gingival inflammation was recorded as follow: 0 = Normal gingiva. 1 = Mild inflammation, slight change in color, slight edema and no bleeding on probing. 2= Moderate inflammation, redness, edema and bleeding on probing. 3= Severe inflammation, marked redness, edema and tendency to spontaneous bleeding.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Inclusion criteria:

  • Patients with periodontitis stage ( Ⅰ & Ⅱ ). Stage I have CAL 1 to 2mm with no tooth loss and probing depth ≤4 mm. Stage II have CAL 3 to 4mm with no tooth loss and probing depth ≤5 mm..

  • Patients who have teeth with both mesial and distal neighboring teeth .

  • Patient with more than 20 natural teeth .

  • Patient free from any systemic disease that may effect the periodontal status according to the criteria of Cornell Medical Index and its modification.

Exclusion Criteria:
  • Long-term therapy with medications within a month prior to enrollment that could affect periodontal status or healing.

  • Pregnant woman and lactating mothers .

  • Patients with a history of traumatic occlusion.

  • Teeth with both endo-perio lesion .

  • Patients with previous periodontal treatment including scaling and root planing and periodontal surgery in the last 3 and 6 months, respectively .

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Principal Investigator: Ahmed Mortada Fikry, professor, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Alzahraa Alghriany, Lecturer, Oral medicine, Periodontology and Oral diagnosis, Faculty of dentistry, Assiut University
ClinicalTrials.gov Identifier:
NCT05928546
Other Study ID Numbers:
  • Quercetin in periodontitis
First Posted:
Jul 3, 2023
Last Update Posted:
Jul 3, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Alzahraa Alghriany, Lecturer, Oral medicine, Periodontology and Oral diagnosis, Faculty of dentistry, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 3, 2023