To Compare and Evaluate the effectiveness of Synthetic Bone Graft Material with and without Injectable Human Blood Clot in the Treatment of Bony Defects in Chronic Gum Disease.

Comparative Clinical and Radiographic Evaluation of Efficacy of G-Graft™ (Hydroxyapatite with Collagen) Versus G-Graft™ (Hydroxyapatite with Collagen) with Injectable Platelet Rich Fibrin in the Treatment of Intrabony Defects in Chronic Periodontitis Patients – A Randomized Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070436

Enrollment

Registered

2024-07-10

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Interventions

Intervention1: Hydroxyapatite with Collagen Alloplastic Graft with Injectable Platelet Rich Fibrin (i- PRF): Hydroxyapatite with Collagen Alloplastic Graft (G-Graft™) with Injectable Platelet Rich Fib

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients in the age group of 30 to 60 years. 2) Patients diagnosed with Chronic Periodontitis. 3) Patients who are non smokers or do not consume tobacco in any other form. 4) Patients are in good systemic health with no contraindication to periodontal surgery. 5) Patients having pocket depths greater than 5mm, intraosseous defect greater than 3mm and with radiographic evidence of vertical/angular bone loss in the affected sites.

Exclusion criteria

Exclusion criteria: 1) One-walled osseous defects. 2) Patients suffering from any systemic diseases or with a compromised immune system. 3) Patients who had received any type of periodontal therapy for the past 6 months. 4) Patients taking immunosuppressant drugs like corticosteroids. 5) Patients with a known history of allergy to Doxycycline or Chlorhexidine or any other medicine used in the study. 6) Patients showing unacceptable oral hygiene compliance during / after Phase I periodontal therapy. 7) Patients taking any drug known to cause gingival enlargement. 8) Pregnant and/or lactating mothers.

Design outcomes

Primary

Measure	Time frame
1. Plaque Index (P.I.) (Tureskey-Gilmore-Glickman Modification of Quigley Hein). 2. Gingival Index (G.I.) (Loe and Silness, 1963) 3. Probing Pocket Depth (PPD) 4. Clinical Attachment Level (CAL)Timepoint: 1) At Baseline 2) After 1 month 3) After 3 month 4) After 6 month	—

Secondary

Measure	Time frame
The radiographic bone fill will be evaluated using Intraoral Periapical Radiographs of the surgical site.Timepoint: Baseline-at baseline. Immediately after the surgery and 6 month post-surgery	—

Countries

India

Contacts

Public ContactDr Mala Dixit Baburaj

Nair Hospital Dental College, Mumbai

maladixit25@gmail.com9223340938

Outcome results

None listed

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