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Comparing Bone Regeneration In The Oral Cavity: Using FDBA With iPRF And FDBA Without iPRF

Comparative Evaluation Of Free Dried Bone Allograft (FDBA) With and Without i-PRF (Injectable Platelet Rich Fibrin) In The Treatment of Human Intrabony Defects- A Clinico-Radiographic Study - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079226
Enrollment
20
Registered
2025-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: K053- Chronic periodontitis Health Condition 2: K053- Chronic periodontitis

Interventions

Intervention1: Group B iPRF with FDBA Group: Ten patients with angular intrabony periodontal defect Follow up for baseline 3 months and 6 months Control Intervention1: Group A FDBA Group: Ten patients

Sponsors

Dr Enakshi Yadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Good level of oral hygiene 2. Subjects of either sex having generalised Chronic Periodontitis 3. Subjects who are systemically healthy with no contraindication to periodontal surgery 4. Presence of PD 5mm in relation to with radiographic evidence of angular bone loss 5. Compliant subjects

Exclusion criteria

Exclusion criteria: 1. Subjects with any systemic disease. 2. Individuals having any deleterious habits such as smoking or tobacco chewing 3. Subjects allergic or sensitive to any medication or any ingredient of the test material 4. Subjects showing unacceptable oral hygiene compliance during or after phase I therapy 5. Pregnant or lactating females 6. Subjects who have undergone any periodontal surgery in the past 6 months

Design outcomes

Primary

MeasureTime frame
To Evaluate And Compare The Reduction In Probing Pocket Depth Of Intrabony Defects With Fdba and iPRF with FDBATimepoint: At Baseline And 6 Months

Secondary

MeasureTime frame
To Evaluate And Compare Gain In Bone Fill Achieved By The above Modalities Using Pre And Post RvgTimepoint: Baseline And 3 Months And 6 Months

Countries

India

Contacts

Public ContactMohd Nazar Rana

Subharti Dental College and Hospital

nazarhasanrana@gmail.com7830070070

Outcome results

None listed

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