Not yet recruiting NCT06637982
Extended Platelet Rich Fibrin in Mandibular Alveolar Ridge Splitting
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: ridge splitting with the use of allograft and pericardium membrane, ridge splitting with the use of extended platelet rich fibrin.
- Who it may be relevant to
- Registry conditions: Ridge Splitting. Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Extended Platelet Rich Fibrin in Mandibular Alveolar Ridge Splitting With Simultaneous Implant Placement
Overview
Thirty two healthy implants will be selected from the outpatient clinic of the oral and maxillofacial department of Mansoura university to be included in this study for replacement of lost posterior teeth with limited bone width.
Interventions
- Procedure ridge splitting with the use of allograft and pericardium membrane
ridge splitting with the use of allograft and pericardium membrane - Procedure ridge splitting with the use of extended platelet rich fibrin
ridge splitting with the use of extended platelet rich fibrin
Primary outcome measures
- implant stability [Time frame: 9 months]
- alveolar ridge width [Time frame: 9 months]
Eligibility criteria
Inclusion criteria
- Patient age 18 years old and older.
- Patient's cooperation, motivation and good oral hygiene.
- Atrophic posterior mandible of horizontal alveolar dimension range between 3 - 6 mm at the crest, with minimum 10 mm vertical height from the alveolar crest to the superior border of the inferior alveolar canal.
- Absence of undercuts in buccal aspect of the ridge.
- Favorable occlusion and no parafunctional habits.
- Patients able to comply with the required recall visits.
- No gender preface in selection of the patients.
- Acceptable inter-arch space for the future prosthesis.
Exclusion criteria
- Any pathological condition at the site of surgery.
- Patients with systemic diseases that contra-indicate the surgical procedure such as uncontrolled diabetes mellitus, bleeding disorders, serious osseous disorders, and mental disorders.
- Patient taking drugs that could affect bone healing process as immunosuppressive drugs and bisphosphonates.
- Heavy smoking and alcoholism.
- Parafunctional habits such as bruxism and clenching.
- Signs of acute infection or pus discharge.
- Untreated periodontal disease or bad oral hygiene.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Mansoura University — Mansoura, Egypt
Identifiers
NCT: NCT06637982 · A0302024OS