The Use of Adhesion Molecule Loaded Hydrogel With Minimally Invasive Surgical Technique in Treatment of Periodontal Intrabony Defect

Periodontitis Clinical Trial

Official title:

The Use of Adhesion Molecule Loaded Hydrogel With Minimally Invasive Surgical Technique in Treatment of Periodontal Intrabony Defect (Randomized Clinical and Biochemical Study)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05653245
• Other study ID #: periodontal regeneration
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: March 15, 2021
• Est. completion date: September 9, 2022

Study information

• Verified date: November 2022
• Source: Minia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary aim of the study is to evaluate efficacy of RGD adhesion molecule loaded hydrogel with minimally invasive surgical technique in treatment of periodontal intrabony defect at baseline and 6months. Secondary outcome is the biochemical evaluation to detect bone morphogenetic proteins level

Description:

Periodontitis is a multifactorial inflammatory disease associated with dysbiotic plaque biofilms and characterized by clinical attachment loss caused by the destruction of the periodontal ligament and loss of supporting bone. One of periodontal therapy goals is regeneration of the lost periodontal attachment apparatus.

. To regenerate healthy periodontal tissue, various clinical techniques were developed to prevent downward epithelial migration and promote periodontal tissue regeneration by the remaining periodontal ligament (PDL) cells or osteoblasts such as open flap debridement (OFD), natural or synthetic filling materials and guided tissue regeneration (GTR).

. Tissue engineering has become one of the most commonly used approaches for bone tissue reconstruction and regeneration, injectable hydrogels have attracted the attention of biomaterials scientists for bone tissue-engineering applications, because they can replace regenerative surgery with a minimally invasive injection method and can form any desired shape, to match irregular defects. Various injectable hydrogels with good moldability and 3D structures have been widely investigated for use in bone tissue engineering.

. Recently a variety of bioactive peptides have been studied and applied for the promotion of bone regeneration to repair local bone defects or treat other bone diseases including extracellular matrix (ECM)- derived peptides, bone morphogenetic proteins (BMPs)-derived peptides and others.

. The arginyl-glycyl-aspartic acid (RGD) peptide is one of bioactive peptides which is the cardinal integrin-binding domain and presents in many extracellular matrix proteins, such as fibronectin and vitronectin. As a part of cell surface signalling, RGD peptide can enhance the expression of osteocalcin (OCN), osteopontin (OPN) and BMP to ensure osteoblast proliferation, differentiation and mineralization.

. The induction of bone depending on the concentration of BMPs which considered important bone biological factors that play essential roles in osteogenesis. BMPs are members of secreted signaling proteins that belong to transforming growth factor beta (TGF-β) superfamily. It has been demonstrated that BMPs induce bone formation by differentiating mesenchymal stem cells to osteoblastic cells

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: September 9, 2022
• Est. primary completion date: February 5, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 55 Years

Eligibility

Inclusion Criteria:

• Patients with diagnosis of periodontitis (stage III or IV and grade B or C) according to new American Academy of Periodontology classification (Tonetti et al., 2018a) (Nguyen et al., 2021).

• Selected patients of both sexes were 20-55 years old.

• All single and multiple rooted teeth in both maxilla and mandible.

• Presence of interdental periodontal pocket with intrabony defect.

• Patients were free from any systemic diseases that could alter their periodontal status, complicate the surgical treatment, or affect healing according to Modified Cornell Index (Abramson, 1966).

• No antibiotics or any medications that affect bone or soft tissue condition were taken during the last six months.

Exclusion Criteria:

• Patients who received regenerative periodontal therapy last 6 months before the initial examination.

• Pregnant or lactating females.

• Smokers were not included as participants in this study.

• Patients not committed to oral hygiene after the re-evaluation of phase I therapy.

• Teeth with mobility more than Grade I.

• Third molars.

Related Conditions & MeSH terms

• Periodontitis
• Tissue Adhesions

Intervention

Drug:
• RGD Peptide
adhesion molecules

Locations

Country	Name	City	State
Egypt	Shaimaa Hamdy	Minya
Egypt	Shaimaa Hamdy	Minya

Sponsors (1)

Lead Sponsor	Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	biochemical evaluation	measure bone morphogenetic protein level in gingival crevicular fluid by ELIST test	1, 7,14 days follow up
Primary	evaluation of intrabony component dimension component dimension	evaluation of intrabony component dimension (defect base fill) length measured by millimeters	6 months follow up
Primary	evaluation of intrabony component dimension	crestal bone level length measured by millimeters	6 months follow up
Primary	evaluation of intrabony component dimension	defect width measured by millimeters	6 months follow up
Secondary	evaluate the clinical parameters attachment gain	The secondary outcomes were to evaluate the clinical attachment gain measured by millimeters	6 months follow up
Secondary	evaluate the clinical parameters	pocket depth reduction measured by millimeters	6 months follow up
Secondary	evaluate the clinical parameters	full-mouth plaque index, full mouth sulcular bleeding index by score	6 months follow up