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Peri implant soft and soft tissue changes around nanopore surface implants with or without platelet rich fibrin (PRF): a clinico-radiographic study

Evaluation of peri implant soft and hard tissue changes around nanopore surface implants with or without platelet rich fibrin (PRF) bioactivation: a clinico-radiographic study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/010196
Enrollment
14
Registered
2017-10-25
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- Patients requiring replacement of teeth with implants

Interventions

Intervention1: Immediate implant placement: Immediate implant placement in freshly extracted socket Control Intervention1: Platelet rich fibrin (PRF) or without PRF activation: Implant surfaces either

Sponsors

Saraswati Dental College Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patient aged more than 18 years who could read, understand and were willing to comply with all the study related procedure after signing an informed consent statement. 2) Systemically healthy subjects having monoradicular tooth as seen in IOPA radiograph indicated for extraction. However, final decision for inclusion in the study was taken after atraumatic extraction. 3) Residual extraction socket possessing intact bone in all dimension (four wall bony defect), jumping gap less than 2 mm (confirmed during surgical phase) and occlusion suitable for planned prosthodontic treatment. 4) Patient who were nonsmoker or had quit smoking from past 2 months (self-reported). 5) The subject sample consisted of patients who required extraction of single rooted tooth and restoration by means of dental implants. 6) The reason for tooth extraction and immediate implant placement were trauma, endodontic and non-restorable carious lesion combined with root or crown fracture. 7) No tooth was removed because of advanced periodontal disease.

Exclusion criteria

Exclusion criteria: 1) Pregnant women or nursing mother and patients using tobacco (smoke/smokeless). 2) Patients with clinically significant or unstable systematic disease affecting bone or soft tissue growth or other renal hepatic, cardiac, endocrine, hematologic, autoimmune, acute or acute infectious disease that contraindicate periodontal surgery . 3) Patients on antibiotic chemotherapeutics, bisphosphonate, allergy, steroid, hormone contraceptives and any other drugs that can effects the bone turn over or immune â?? inflammatory response in last 6 months. 4) Presence of any chronic systemic disease (example diabetes mellitus), allergy, immuno-suppression, previous history of hospitalization in one year, ongoing chemo/radiotherapy or a history of drug abuse. 5) Presence of chronic pain, purulent periodontal and endodontic lesion as well as severe periodontal bone loss with a remaining alveolar height of less than 7mm.

Design outcomes

Secondary

MeasureTime frame
Implant SurvivalTimepoint: implant survival till 9 months post loading of implants

Primary

MeasureTime frame
Plaque index, Gingival index, Bone lossTimepoint: Up to 9 months after loading of implants.

Countries

India

Contacts

Public ContactDr Vivek Kumar Bains

Saraswati Dental College, Lucknow

doc_vivek76@yahoo.co.in

Outcome results

None listed

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