Autogenous Dentin Derived Barrier Membrane Versus Collagen Membrane

Autogenous Dentin Derived Barrier Membrane Versus Collagen Membrane for Guided Bone Regeneration in Immediate Implant

Status

Active, not recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06615362

Acronym

DDBM dental

Enrollment

Registered

2024-09-26

Start date

2022-04-10

Completion date

2024-10-10

Last updated

2024-09-26

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

Conditions

IMMEDIATE IMPLANT, TOOTH EXTRACTION

Brief summary

Autogenous Dentin Derived Barrier Membrane versus Collagen Membrane

Detailed description

Autogenous Dentin Derived Barrier Membrane versus Collagen Membrane for Guided Bone Regeneration in Immediate Implant

Interventions

PROCEDUREpreparation of dentin membrane from hopeless tooth for Guided Bone Regeneration in Immediate Implant

tooth extraction , preparation of dentin membrane ,immediate implantation ,Xenogeneic bone graft material, application of dentin derived barrier membrane

PROCEDURECollagen Membrane for Guided Bone Regeneration in Immediate Implant

like group one but with application of collagen membrane

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Two arms: one arm Autogenous Dentin Derived Barrier Membrane ,second arm Collagen Membrane .

Eligibility

Sex/Gender

ALL

Age

18 Years to 50 Years

Healthy volunteers

Yes

Inclusion criteria

1. Patient's age ranges from 18-50 years. 2. Adequate inter-arch relation and inter-occlusal space that could accommodate the implant abutment and the future restoration 3. Non-restorable tooth that needs dental extraction & guided bone regeneration for immediate implant. 4. Presence of alveolar bone defect with vertical loss of buccal bone more than a third implant thread. 5. Co-operative patients willing to complete the follow-up periods.

Exclusion criteria

1. Any pathological condition at site of surgery. 2. Patients with systemic diseases that contra-indicate the surgical procedure. 3. Heavy smoking. 4. Parafunctional habits such as bruxism and clenching. 5. Pregnant patients. -

Design outcomes

Primary

Measure	Time frame	Description
All patients were evaluated radiographically immediately postoperative,and after 12 months	1 year	Radiographic Evaluation Cone Beam Computed Tomography scan was taken to measure Marginal Bone loss and Relative bone density

Countries

Egypt

Outcome results

None listed

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