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A study to compare demineralized freeze dried bone allograft with or without barrier membrane in treatment of periodontal disease.

An Evaluation of Demineralized Freeze Dried Bone Allograft with or without Amnion membrane in Treatment of Grade II Furcation Defects- A Clinical and CBCT Study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/01/006531
Enrollment
20
Registered
2016-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Periodontitis.

Interventions

Intervention1: The trial is an Interventional trial in the treatment of chronic periodontitis comparing two different treatment modalities one involving the placement of Demineralized Freeze Dried bon

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with moderate to advanced periodontitis as assessed by probing pocket depth >= 5 mm and clinical attachment level >= 5 mm 2. Patients with atleast one pair of bilateral grade II furcation defect in either maxillary or mandibular arch.

Exclusion criteria

Exclusion criteria: 1. Subjects with history of systemic diseases, allergies or drug usage. 2. Subjects who have undergone periodontal treatment in previous 6 months

Design outcomes

Primary

MeasureTime frame
Improvement in Periodontal Status i.e. reduction in Probing Pocket Depth, gain in Clinical Attachment Level, Bone Fill in Furcation area (seen by advanced radiography i.e. CBCT) within 3 to 6 monthsTimepoint: Improvement in Periodontal Status i.e. reduction in Probing Pocket Depth, gain in Clinical Attachment Level, Bone Fill in Furcation area (seen by advanced radiography i.e. CBCT) within 3 to 6 months

Secondary

MeasureTime frame
Reduction in Plaque scores and Gingival Bleeding scores representing improvement in Gingival (soft tissue) status, within 3-6 months.Timepoint: Reduction in Plaque scores and Gingival Bleeding scores representing improvement in Gingival (soft tissue) status, within 3-6 months.

Countries

India

Contacts

Public ContactDr Abhay P Kolte

VSPM Dental College and Research Centre

drabhaypkolte@gmail.com09011071467

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026