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Injectable Platelet-Rich Fibrin As An Adjunct To Minimally Invasive Nonsurgical Treatment In Endodontic-Periodontal Lesions: A Randomized Controlled Trial

NCT07928856 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-12-01
Last updated
2026-11-10

Condition(s) studied

Endodontic-Periodontal Lesions

Investigational drug(s) / intervention(s)

Non-invasive application of i PRFNon-surgical endodontic and periodontal treatment

Non-invasive application of i PRF: Non-invasive application of i PRF in endodontic-periodontal lesions

Non-surgical endodontic and periodontal treatment: Non-surgical endodontic treatment followed by non-surgical periodontal treatment

Study summary

To compare the effect of non-invasive injectable PRF application on periodontal healing in Grade 2-3 endodontic periodontal lesions.

Hypothesis: No difference in healing outcome between the two groups. Outcome measure 1: (Primary outcome)

Periodontal healing as demonstrated by change in Clinical Attachment Level (CAL)

Secondary outcomes:

* Change in Pocket probing depth (PPD)
* Radiographic defect fill at 6 months using digital periapical radiographs compared to baseline.
* Gingival recession
* Tooth mobility
* Bleeding on Probing (BoP)
* Plaque index
* Patient reported outcomes (VAS pain scores)
* Number of analgesics consumed
* Cost of treatment
* Quality of life questionnaire

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: Presence of a periodontal-endodontic lesion (EPL without root damage in non-periodontitis patients) according to (Herrera et al., 2018) confirmed by: * A negative response to pulp sensibility test * Deep periodontal pockets (≥5 mm) reaching or close to the apex (EPL Grade 2 or 3) according to the classification by (Herrera et al., 2018). * Absence of root damage Exclusion Criteria: * • Presence of one narrow deep periodontal pocket around the affected tooth (EPL Grade 1) * Presence of any type of root damage such as root fracture, perforation or resorption * Presence of crowns or fixed prosthesis * History of fractured teeth * Occlusal abnormality * Periodontal therapy for the last 3 months * Presence of systemic diseases affecting periodontal healing * Smoking

Primary outcome measure(s)

  • Clinical Attachment Level — 6 months
    Periodontal parameters will be measured using UNC periodontal probe

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Cairo University Cairo Cairo Governorate
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07928856 on ClinicalTrials.gov ↗ ← All trials in Egypt