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Bovine Bone With or Without Concentrated Growth Factor in the Treatment of Chronic Periodontitis

Comparative Study Between Bovine Bone With or Without Concentrated Growth Factor in the Treatment of Chronic Periodontitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07108790
Enrollment
20
Registered
2025-08-07
Start date
2022-03-01
Completion date
2025-01-01
Last updated
2025-08-07

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

Conditions

Bovine Bone, Chronic Periodontitis, Concentrated Growth Factor

Brief summary

The aim of this study is to compare bovine bone with or without concentrated growth factor in the treatment of chronic periodontitis.

Detailed description

Periodontitis is an infection-driven inflammatory disease resulting from dental plaque accumulation at the gingival margin, triggering an inflammatory response that leads to microbial alterations and may have severe consequences for the periodontium of susceptible individuals. The xenograft most commonly used in periodontal regeneration procedures is the deproteinized bovine or equine bone mineral. Platelets are known to play a significant role in guided tissue regeneration (GTR) by releasing several growth factors, such as platelet-derived growth factor (PDGF), and plasma rich in growth factors (PRGF), which are present in platelet-rich plasma (PRP), a first-generation platelet concentrate. Platelet-rich fibrin (PRF) and concentrated growth factors (CGF) are considered the second generation of platelet concentrate.

Interventions

OTHERConcentrated growth factors, collagen membrane and xenograft bone graft

Ten sites were treated by concentrated growth factors (CGF), collagen membrane, and xenograft bone graft.

OTHERCollagen membrane and xenograft bone graft

Ten sites were treated with a collagen membrane and a xenograft bone graft.

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Presence of angular periodontal intra-bony defects with a pocket depth (PD) ≥ 5mm. * Optimal compliance as evidenced by no missed treatment appointments and a positive attitude towards oral hygiene. * Full-mouth bleeding score ≤ 25%.

Exclusion criteria

* Patients with relevant medical conditions that may affect periodontal regeneration and periodontal surgery. * Patients who have any disease or take any medication that affects the normal number or function of platelets. * Smokers. * Pregnant or lactating women. * Patients in whom periodontal surgery had previously been carried out on the selected site. * Patients with aggressive periodontitis.

Design outcomes

Primary

MeasureTime frameDescription
Probing Pocket depth6 months post-procedureProbing Pocket depth (PPD) was measured.

Secondary

MeasureTime frameDescription
Clinical attachment level6 months post-procedureClinical attachment level (CAL) was measured.
Bleeding on probing6 months post-procedureBleeding on probing (BOP) was measured.
Plaque index6 months post-procedurePlaque index (PI) was measured.

Countries

Egypt

Outcome results

None listed

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