Efficacy of Artificial Bone in Angular Bone Loss

Evaluation of efficacy of Xenograft in intrabony defect: A Clinico-Radiographic study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/05/014239

Enrollment

Registered

2018-05-30

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- angular bone loss in jaw

Interventions

Intervention1: Xenograft in intrabony defect: Bovine bone graft placed in angular bone defect of more than 3 mm Total duration of therapy was 6 months Control Intervention1: not applicable: not applic

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects should be non smoker 2 Subjects should have no systemic disease 3 Sites with infrabony pocket depth of greater than or equal to 6 mm (at least at one site) 4 Sites with clinical attachment loss of greater than or equal 4 mm

Exclusion criteria

Exclusion criteria: 1 Patient who cannot maintain good oral hygiene 2 Patient who are known allergic to bone graft material 3 Pregnant women or lactating mothers

Design outcomes

Primary

Measure	Time frame
pocket depth clinical attachment level bone fillTimepoint: baseline 3 months 6 months	—

Secondary

Measure	Time frame
gingival index plaque indexTimepoint: base line 3 months 6 months	—

Countries

India

Contacts

Public ContactSheetal Surjeet

Sri Rajiv Gandhi college of Dental sciences and Hospital

drsaritanarayan@yahoo.com9845112838

Outcome results

None listed

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