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RGD With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defect (MINST + RGD)

M

Minia University

Status

Not yet enrolling

Conditions

Periodontal Diseases
Alveolar Bone Loss
Intrabony Defect

Treatments

Drug: RGD Peptide

Study type

Interventional

Funder types

Other

Identifiers

NCT06936605
committee 1051 (Other Identifier)
MINST+ RGD in Periodontitis

Details and patient eligibility

About

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.

Full 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

Enrollment

45 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 3 patient groups, including a placebo group

negative control group
Placebo Comparator group
Description:
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique
Treatment:
Drug: RGD Peptide
control group
Placebo Comparator group
Description:
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique with placebo hydrogel
Treatment:
Drug: RGD Peptide
study group
Active Comparator group
Description:
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique with RGD hydrogel
Treatment:
Drug: RGD Peptide

Trial contacts and locations

0

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Central trial contact

shaimaa Hamdy, lecturer of Periodontology

Data sourced from clinicaltrials.gov

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