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NCT07042204

Effectiveness of E-prf Alone and in Combination With Bioactive Glass Nanoparticles in Grade II Furcation Defects

Completed NA Last updated 13 January 2026
What this trial tests

NA trial testing Group I (extended platelet-rich fibrin) in Furcation Defects in 30 participants. Completed in 3 August 2025.

Timeline
3 January 2024
Primary endpoint
3 June 2025
3 August 2025

Quick facts

Lead sponsorMerna Nasser Mohamed Mostafa Ibrahim Elnahas
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment30
Start date3 January 2024
Primary completion3 June 2025
Estimated completion3 August 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Merna Nasser Mohamed Mostafa Ibrahim Elnahas

Who can join

Adults 18 to 50, any sex, with Furcation Defects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to evaluate and compare the effectiveness of extended platelet-rich fibrin (ePRF) alone and in combination with bioactive glass nanoparticles in the treatment of grade II furcation defects clinically and radiographically.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Furcation Defects

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07042204.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing