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RGD With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defect

The Use of Integrin Binding Domain Loaded Hydrogel (RGD) With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defect (Randomized Clinical Trial Study)

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06936605
Acronym
MINST + RGD
Enrollment
45
Registered
2025-04-20
Start date
2025-04-15
Completion date
2025-10-20
Last updated
2025-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Loss, Intrabony Defect, Periodontal Diseases

Keywords

MINST, RGD, intrabony defect

Brief summary

Periodontal regeneration is a complex process that involves coordinated activities and interactions of many cell types, extracellular matrix, cytokines, and specific growth factors to restore tissue integrity. The most important challenge facing periodontal regeneration is cellular insufficiency. Periodontal defects usually have a limited regenerative capacity due to their bounded surface area which is supposed to provide the wound area with a limited number of viable cells and a limited amount of biologic mediators. Cell recruitment and adhesion into the defect area are essential for cells to survive and secrete collagen. Apoptosis is initiated when failure in adhesion in many different cell types occurs. Some periodontal treatment options failed in the reconstruction of the defect due to failure in wound stabilization and subsequent cell adhesion. Many treatment options have been developed to enhance defect stability and cellular recruitment including the use of GTM and different biologics. However, the treatment outcomes vary considerably depending on the level of the defect cellularity and the degree of cell recruitment into the defect area. For maximum outcomes, enhanced stability, vascularity, and biologics-sustained delivery were suggested. The minimally invasive surgical technique (MIST) suggested by Cortellini et al. offers a suitable level of tissue preservation that could help in defect stability and cellular adhesion. It was suggested to promote flap stability, maintain space, and maintain a greater amount of blood supply at the alveolar crest and papillary levels.

Detailed description

Periodontitis is an inflammatory multifactorial disease initiated by pathogenic bacteria accumulated as a biofilm on the tooth surface leading to clinical attachment loss (CAL), pocket formation (PD), bleeding on probing (BOP), and bone loss which if neglected may lead to increased tooth mobility and final tooth loss. Pathological tooth mobility may arise from extensive alveolar bone loss, traumatic occlusion, acute periodontal inflammation, and apical tooth displacement. Treating tooth mobility can be a challenging process, particularly for patients with severe periodontitis, including those in stage III or IV, who often experience a range of these symptoms. ue to compromised periodontal support. Therefore, effective treatment not only relies on periodontal therapy but also on occlusal stability and tooth splinting

Interventions

RGD peptide is an integrin binding site

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

patients do not know the type of treatment and outcomes assessor does not know type of group

Intervention model description

Groups and intervention: Patients selected in this study will be classified into three groups: * Group 1: Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with modified minimally invasive surgical technique (MINST) and RGD hydrogel injection. * Group 2: Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with (MINST) and hydrogel injection. * Group : Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with (MINST) alone. Postoperative phase: 1. Routine verbal and written postoperative instructions will be given to all patients. 2. Patients will be advised to refrain from retracting the cheeks, to accomplish food mastication in areas away from surgical site, and to avoid brushing the area in the first week.

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* • All patients included will have moderate to advanced periodontitis. * Patients included in this study will be free from any systemic diseases according to criteria of Modified Cornell Medical Index(10). * Patients who had not undergone any type of regenerative periodontal therapy six months prior to the initial examination.

Exclusion criteria

* • Patients with systemic diseases, smokers, pregnant (female). * Patients received antibiotics or non-steroidal anti-inflammatory drugs six months before the beginning of the study.

Design outcomes

Primary

MeasureTime frameDescription
CAL by millimetersbaseline, 3months and 6 monthsMeasure clinical attachment loss pre and after-intervention

Contacts

Primary Contactshaimaa Hamdy, lecturer of Periodontology
shimaa.3m.sh@gmail.com+201030576405

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026