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Not yet recruitingNCT06936605MINST + RGDUpdated Apr 20, 2025

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

An interventional study of RGD Peptide in Intrabony Defect, Periodontal Diseases and Alveolar Bone Loss, sponsored by Minia University. Not yet recruiting. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2025-04-20.

Sponsored by Minia University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study 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.

Read the 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

02

Conditions studied

  • Intrabony Defect
  • Periodontal Diseases
  • Alveolar Bone Loss

Keywords

  • MINST
  • RGD
  • intrabony defect
03

In context

Alveolar Bone Loss

297 studies on the registry are indexed under Alveolar Bone Loss; 76 are open to participants now.

This study's planned enrollment of 45 is above the median of 25 across 254 interventional studies indexed under Alveolar Bone Loss.

Browse Alveolar Bone Loss studies →

Lead sponsor

Minia University is the lead sponsor of 356 studies on the registry; 115 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts 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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
45 participants (estimated)

Study arms

  • Placebo comparator
    negative control group

    Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique

    Drug: RGD Peptide

  • Placebo comparator
    control group

    Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique with placebo hydrogel

    Drug: RGD Peptide

  • Active comparator
    study group

    Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with minimally invasive non-surgical technique with RGD hydrogel

    Drug: RGD Peptide

Interventions

  • DrugRGD Peptide

    RGD peptide is an integrin binding site

06

What researchers measure

Primary outcomes

  1. CAL by millimeters

    Measure clinical attachment loss pre and after-intervention

    Time frame: baseline, 3months and 6 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — after complete study and publishing all data well be available

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06936605
Lead sponsor
Minia University
Responsible party
shaimaa hamdy (lecturer in periodontology, Minia University) — Principal investigator
First posted
Apr 20, 2025
Start date
Apr 15, 2025 (estimated)
Primary completion
Sep 20, 2025 (estimated)
Completion
Oct 20, 2025 (estimated)
Last update
Apr 20, 2025

Study contacts

shaimaa Hamdy, lecturer of Periodontology
Contact
shimaa.3m.sh@gmail.com
+201030576405 ext. +201555035523

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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