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Regenerative Potential of Cultured Gingival Fibroblast- Mesenchymal Stem Cells in Treatment of Periodontitis

Clinical Regenerative Potential of Cultured Gingival Fibroblast- Mesenchymal Stem Cells in Treatment of Periodontal Intrabony Defects (Randomized Clinical and Biochemical Trial)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03638154
Enrollment
20
Registered
2018-08-20
Start date
2016-03-15
Completion date
2018-02-22
Last updated
2018-08-20

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

Conditions

Periodontal Intrabony Defect

Brief summary

clinical trial was conducted to evaluate regenerative potentials of cultured gingival fibroblasts and GMSCs carried in beta tri calcium phosphate scaffold into intrabony periodontal defects in human by clinical and radiographic parameters

Detailed description

In the present study, twenty posterior two or three osseous intrabony periodontal defects were involved . They were grouped in to two groups. Group I included ten intrabony posterior defect received beta tri calcium phosphate (β TCP) bone substitute. Group II included ten posterior intrabony periodontal defect and they received a mixture of gingival fibroblast(GF) and gingival mesenchymal stem cells(GMSCs) carried on a vehicle of β TCP covered by a resorbable collagen membrane. CBCT was used preoperatively and after 6 months for hard tissue evaluation. PDGF and BMP were measured in GCF at days 1,3,7,14.

Interventions

PROCEDUREGF+GMSCs carried on β TCP

surgical augmentation of GF+GMSCs carried on β TCP in intrabony periodontal defect and covered by collagen membrane(Bioresorb, Sybron, implant solutions GmbH Bremen, Germany) Cytoplast, RTM Collagen Cytoplast, Barrier Membranes, Osteogenics Biomedical, New Gersey, USA). Ibuprofen

PROCEDUREβ TCP bone substitute only

surgical augmentation by β TCP in intrabony periodontal defect(Bioresorb, Sybron, implant solutions GmbH Bremen, Germany) Ibuprofen

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
32 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Presence of interproximal osseous defects estimated from radiographic evaluation (Cone Beam CT) and transgingival bone sounding ≥3mm of two or three osseous walls. * Probing Depth ≥5mm after initial therapy. * Attachment loss ≥4mm. * full mouth plaque score and bleeding on probing score ≤ 20% after phase I therapy. * non vital teeth only involved. * no furcation involvement of the teeth presenting the intraosseous defects. * Thick gingival biotype more than 1 mm with enough width of attached gingiva. * Accepts Healthy Volunteers

Exclusion criteria

* Patients with systemic disease or compromised immune illness using Cornell medical index * Smoker's patients. * Pregnant and lactating females. * Uncooperative patients (low compliance, bad oral hygiene). * Decision impaired individuals (prisoners, handicapped and mentally retarded patients).

Design outcomes

Primary

MeasureTime frameDescription
bone gain in periodontal defects(by mm)6 months20 patients were involved as assessed by cone beam ct at baseline (pre) and 6 months later(post). the fusion of pre and post operative cone beam ct scan of the intrabony periodontal defect to measure bone gain by mm. so that, the regenerative potentials of cultured gingival into ten intrabony defect fibroblasts and GMSCs carried by tri calcium phosphate , the bone gain was measured by radiographic fusion of pre and post image of intrabony periodontal defects in human.

Secondary

MeasureTime frameDescription
the regenerative power of the defect was evaluated by growth factor concentration in GCF.day 1,3,7,14 after surgery4 GCF samples were collected from each patient at day 1,3,7,14 after periodontal surgery then a Biochemical analysis of BMP-2 and PDGF-bb (by mg /dl) concentrations in GCF by using ELIZA kite which reflect the healing power at the initial periods of healing in different groups.

Outcome results

None listed

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