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Recruiting NCT06757218

NCT06757218 Post Extraction Changes After Alveolar Socket Preservation Using Autogenous Dentin Graft (ADG) Combined With Either Albumin Platelet-rich Fibrin (ALB-PRF) or Standard Platelet-rich Fibrin (PRF).

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Clinical Trial Summary
NCT ID NCT06757218
Status Recruiting
Phase
Sponsor Kafrelsheikh University
Condition Alveolar Socket Preservation
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-06-01
Primary Completion 2026-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
empty socketAutogenous Dentin Graft with Platelet Rich FibrinAutogenous Dentin Graft with Albumin Platelet Rich Fibrin

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2025-06-01 with a primary completion date of 2026-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The study focuses on the impact of tooth loss on alveolar bone, which shrinks significantly within the first three months. To prevent this, strategies like alveolar ridge preservation are used. Autogenous dentin, taken from the patient, supports healing and bone regrowth. Platelet-rich fibrin (PRF), made from the patient's blood, enhances healing and bone density by releasing growth factors. A new technique combining L-PRF with albumin creates a stable healing membrane that provides a steady release of growth factors. Overall, these methods improve recovery after tooth extractions and prepare sites for future dental work.

Eligibility Criteria

Inclusion Criteria: * Medically free patients. * Adult patients above 18 Years to 60 Years. * Non-restorable tooth indicated for extraction. * Posterior mandibular teeth. * Inactive infection related to the tooth. * Cooperative patients. Exclusion Criteria: * Presence of any systemic disease that could influence the outcome of the therapy. * Presence of any risk factor (smoker, pregnant and lactating patients). * Patients with bone diseases. * Patients with poor oral hygiene.

Contact & Investigator

Central Contact

MUATH ATIF HASSAN

✉ muath_01pg@den.kfs.edu.eg

📞 +201507571780

Principal Investigator

Enas Ahmed Elgendy, PhD

STUDY DIRECTOR

Kaferelsheikh University

Frequently Asked Questions

Who can join the NCT06757218 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Alveolar Socket Preservation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06757218 currently recruiting?

Yes, NCT06757218 is actively recruiting participants. Contact the research team at muath_01pg@den.kfs.edu.eg for enrollment information.

Where is the NCT06757218 trial being conducted?

This trial is being conducted at Kafr ash Shaykh, Egypt.

Who is sponsoring the NCT06757218 clinical trial?

NCT06757218 is sponsored by Kafrelsheikh University. The principal investigator is Enas Ahmed Elgendy, PhD at Kaferelsheikh University. The trial plans to enroll 60 participants.

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