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Evaluation of Autogenous Demineralized Dentin Graft for Ridge Preservation With and Without Injectable Platelet Rich Fibrin

Clinical and Radiographic Evaluation of Autogenous Demineralized Dentin Graft for Ridge Preservation With and Without Injectable Platelet Rich Fibrin (A Randomized Controlled Clinical Trial)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05437172
Enrollment
24
Registered
2022-06-29
Start date
2022-06-30
Completion date
2023-12-15
Last updated
2025-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Loss, Dentin Graft, Ridge Preservation

Brief summary

Ridge preservation should be considered whenever possible after tooth extraction. Whether implant placement would be performed or for aesthetic consideration at pontic sites when conventional bridge is planned. Ridge preservation aims to maximize the bone formation accompanied with good soft tissue architecture to facilitate implant and prosthetic replacement restoring function, phonetics and aesthetics. the Aim of the study is To evaluate the bucco-lingual ridge width clinically and radiographically, height of buccal and lingual ridges of the socket after application of injectable platelet rich fibrin and autogenous dentin graft.

Interventions

PROCEDUREinjectable platelet rich fibrin with demineralized dentin graft

after atraumatic extraction, collection of whole venous blood (9 ml) in sterile vacutainer tubes will be done without anticoagulant added, vacutainer tubes will be then placed in a centrifugal machine at 700 revolutions per minute (rpm) for 3 min with a tube filled with water to maintain the balance during the centrifuging process. ADDG particles prepared by demineralization of tooth particles in 0.6N hydrochloric acid for 30 min to achieve demineralization then washed twice in saline and dried with sterile gauze. Graft particles will be loaded at the defect site to restore ridge form, large metal condenser was used to adapt the graft to the defect and stabilizing the graft with sutures.

PROCEDUREdemineralized dentin graft

after atraumatic extraction, ADDG particles will be prepared by demineralization of tooth particles in 0.6N hydrochloric acid for 30 min to achieve demineralization then washed twice in saline and dried with sterile gauze. Graft particles will be loaded at the defect site to restore ridge form, large metal condenser was used to adapt the graft to the defect and stabilizing the graft with sutures.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 18 years need of at least one single rooted tooth extraction. * Non-restorable teeth. * Systemically healthy patients. * Good oral hygiene, Plaque index less than 15%. * Non-smoker or Smoking ≤ 10 cigarettes/day. * Cooperative patients able and accept to come for follow up appointments.

Exclusion criteria

* Any interim intervention that may have affected any of the outcomes of interest. * Pregnant and lactation females. * Smoking ˃ 10 cigarettes/day. * Patients reporting systemic conditions that may compromise healing or bone metabolism (eg: diabetes). * Patients with poor oral hygiene. * Any known allergies.

Design outcomes

Primary

MeasureTime frameDescription
Radiographic Bucco-lingual ridge width changeup to 24 weeksradiographic measurement

Secondary

MeasureTime frameDescription
Changes in the height of the socket buccal and lingual ridges.up to 24 weeksradiographic measurement
postoperative painimmediately after the procedureVisual analogue scale from zero (better) to 10 (worse)
Patient satisfactionimmediately after the procedurebinary yes and no
Keratinized tissue widthup to 24 weeksperiodontal probe measurement
chair timeimmediately after the procedurein minutes

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026