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Platelet-rich fibrin in immediate implants with buccal bone defect

Evaluation of the effect of i-prf and Allograft bone substitute combination in bone regeneration around immediate implants with buccal bone dehiscence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220407054448N1
Enrollment
20
Registered
2022-05-08
Start date
2022-03-09
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Buccal bone defect. Other specified diseases of jaws

Interventions

Intervention 1: Intervention group: 10 patients who after implanting, allograft with platelet-rich fibrin was used in buccal defect regeneration. Intervention 2: Control group: 10 patients who after i

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: hopeless single root teeth extracted due to trauma, caries, resorption and root fracture age over 20 years old good oral hygiene : FMBS,FMPS < 25% Buccal gap between socket wall and fixture more than 2 mm plus a small dehiscence defect in buccal healthy soft tissue

Exclusion criteria

Exclusion criteria: severe atrophy of ridge active infection (on periodontium or mucosa) patient with history of radiotherapy or chemotherapy use of alcohol or cigarrete more than 10 pieces a day patient with systemic disorders ( uncontrolled diabetes, autoimmune disorders, etc..) pregnancy patient with bone, or hematologic disorders presence of periapical pathology which involves adjacent teeth

Design outcomes

Primary

MeasureTime frame
Dimension of buccal bone plate. Timepoint: 6 months from immediate implantation. Method of measurement: cone beam computed tomography (CBCT).;Bone density. Timepoint: 6 months from immediate implantation. Method of measurement: cone beam computed tomography (CBCT).;Implant stability value. Timepoint: 6 months from immediate implantation. Method of measurement: periotest device.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactvahid esfahanian

Islamic Azad University

mhs.ahmadishadmehri@gmail.com+98 31 3500 2141

Outcome results

None listed

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