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To evaluate and compare immediate implant placement along with provisionalization with and without Concentrated Growth Factor-enriched bone graft

Comparative evaluation of immediate implant placement & provisionalization with and without CGF-enriched bone graft A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030848
Enrollment
30
Registered
2021-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: Y998- Other external cause status Health Condition 2: Y998- Other external cause status

Interventions

Intervention1: Immediate implant placement with provisionalization: This is an interventional study in which the effect of immediate implant placement & provisionalization with and without CGF-enriche

Sponsors

Dr Vinisha Bajaj
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA 1 Systemically healthy patients 2 Patient with healthy and stable soft tissue architecture 3 Sites at which minimum torque of 35 Ncm is obtained at the time of implant insertion 4 Co-operative motivated and hygiene conscious patients 5 Tooth/teeth with Grade I or II mobility required to be extracted 6 Root stumps 7 Tooth with endodontic failure or non-restorable caries or vertical fracture

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA 1 General contraindications to implant surgery 2 Patients with a history of irradiation in the head and neck area within the last 6 months 3 Treated or under treatment with intravenous amino-bisphosphonates 4 Smokers or patients with poor oral hygiene 5 Patients with para-functional habits 6 Pregnant or lactating females

Design outcomes

Primary

MeasureTime frame
hard and soft tissue changes clinically at baseline 3 & 6 months and radiographically using CBCT at baseline & 6 months post operativelyTimepoint: baseline 3 and 6 months

Secondary

MeasureTime frame
Soft tissue assessment with Testori Implant Esthetic Score Bleeding on probing Probing depth Patient satisfaction using VAS scale Timepoint: baseline 3 and 6 months

Countries

India

Contacts

Public ContactDr Abhay Kolte

VSPM Dental College & Research Centre

drabhaypkolte@gmail.com09011071467

Outcome results

None listed

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