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NCT Number: NCT07613606

Injectable Platelet-Rich Fibrin With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defects

This study aims to clinically and radiographically evaluate the adjunctive effect of injectable platelet-rich fibrin (i-PRF) used in combination with a minimally invasive non-surgical technique for the regenerative treatment of intrabony periodontal defects.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

October 6 University

Cairo, 12511, Egypt

Location status: Recruiting

Location contact

Amany A Alaraby, MD

SUB_INVESTIGATOR

Amir R Elngar, B.D.S

CONTACT

[email protected]

00201004634587

Reham L Aggour, MD

SUB_INVESTIGATOR

About this study

Periodontitis is a chronic inflammatory disease characterized by the progressive destruction of the periodontal supporting tissues, ultimately leading to tooth loss if left untreated.

Optimal periodontal regeneration within intrabony defects depends on the preservation of soft tissues and the maintenance of primary wound closure. Minimally invasive non-surgical periodontal therapy (MINST) has been introduced as a concept aiming to obtain extensive subgingival debridement with minimal tissue trauma.

Platelet-rich plasma (PRP) is an autologous blood product which is created through the centrifugation process of whole blood. It is defined as having a platelet concentration above that of normal physiological levels. The platelets present in PRP carry granules containing a significant number of active biomolecules.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients of both genders >18 years old, medically free of systemic diseases affecting periodontal regeneration.
  • Diagnosis of 'periodontitis' stage III (grades B or C).
  • Single-rooted and multi-rooted vital teeth in either the maxilla or the mandible.
  • Presence of comparable bilateral two- or three-walled intrabony defects [probing pocket depth (PPD), > 5 mm with intrabony defect depth ≥ 3 mm, from the alveolar crest to the defect base, at screening radiograph] not in a furcation-involved tooth.

Exclusion criteria

  • Patients with systemic illness known to affect the outcome of periodontal therapy, including diabetes, immune deficiencies, etc.
  • Pregnant and lactating women
  • Current use of any form of tobacco.
  • Non-surgical periodontal treatment in the past 6 months, or surgical periodontal treatment in the past 12 months.
  • Degree 2 or 3 mobility of the involved sites.6.
  • Presence of periapical pathology, acute infection, or subgingival restoration which could interfere with clinical measurements.

Treatment and study plan

Minimally invasive non-Surgical technique

Procedure

Patients will receive minimally invasive non-Surgical technique (MINST) alone

Minimally invasive non-Surgical technique + platelet-rich fibrin

Procedure

Patients will receive minimally invasive non-Surgical technique (MINST)+ injectable platelet-rich fibrin (i-PRF) injection

Primary outcomes

  1. Presence of comparable bilateral-walled intrabony defects

    Time frame: 6 months postoperatively

    Assessment of intrabony defect fill radiographically will be measured using the standardized paralleling technique.

    Presence of comparable bilateral-walled intrabony defects (PPD, > 5 mm with intrabony defect depth ≥ 3 mm, from the alveolar crest to the defect base, at screening radiograph) not in a furcation-involved tooth.

Secondary outcomes

  1. Clinical attachment level

    Time frame: 6 months postoperatively

    Clinical attachment level (CAL) will be measured in millimeters from the cemento-enamel junction (CEJ) to the base of the periodontal sulcus at 6 sites per tooth

  2. Interproximal probing depth

    Time frame: 6 months postoperatively

    Probing depth (PD) will be measured in millimeters from the gingival margin to the base of the periodontal sulcus at 6 sites per tooth

  3. Gingival margin

    Time frame: 6 months postoperatively

    Gingival margin will be measured from the cemento-enamel junction (CEJ).

  4. Bleeding on probing

    Time frame: 6 months postoperatively

    Bleeding on Probing (BoP) will be measured using papillary bleeding index that is induced by gentle manipulation of the tissue at the depth of the gingival sulcus

  5. Plaque index

    Time frame: 6 months postoperatively

    Plaque index (PI) will be measured for estimating the status of oral hygiene by measuring dental plaque that occurs in the areas adjacent to the gingival margin

Study contacts

Contact information is provided by the study sponsor or research team.

Amir R Elngar, B.D.S

CONTACT

[email protected]

00201004634587

Sponsors and collaborators

Lead sponsor

October 6 University

Other

Registry information

Official study title

Injectable Platelet-Rich Fibrin (i-PRF) With Minimally Invasive Non-Surgical Technique in Treatment of Periodontal Intrabony Defects: A Randomized Clinical Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 29, 2026
Registry last updated
May 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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