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To compare the buccal bone augmentation using bone ring and particulate bone graft

Comparative evaluation of bone ring and particulate bone graft using CBCT in buccal bone augmentation with simultaneous implant placement - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093762
Enrollment
24
Registered
2025-08-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: T149- Unspecified injury

Interventions

Intervention1: Xenograft Bone Ring: Buccal bone augmentation with xenograft bone ring after 6 months. Control Intervention1: Xenograft Particulate Bone graft: Buccal bone augmentation with particulate

Sponsors

Priyadharshini AS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Individuals willing to offer the voluntary informed consent to participate in the study. 2)Age ranging between 20-60 years. 3)Both male and female. 3)Systemically healthy individuals. 4)Partially edentulous.

Exclusion criteria

Exclusion criteria: 1)Individuals with any form of systemic illness. 2)Individuals who are not willing to offer the voluntary informed consent to participate in the study. 3)Individuals receiving antibiotic therapy or non-steroidal anti-inflammatory drugs during the previous two months. 4)Individuals under periodontal treatment. 5)Use of oral topical agents like mouthwash, gum paints before 3 months and during the study.

Design outcomes

Primary

MeasureTime frame
Buccal bone height and widthTimepoint: At 6 months—

Secondary

MeasureTime frame
Soft tissue gainTimepoint: At 3 months—

Countries

India

Contacts

Public ContactDr Aniz A

Karpaga Vinayaga Institute of Dental Sciences

anizmds@gmail.com9884233240

Outcome results

None listed

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