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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03037125
Other study ID # PERIO 3:7:3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date June 1, 2019

Study information

Verified date May 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Split crest technique is a technique for horizontal bone augmentation used in case of narrow alveolar ridges as an alternative to the more aggressive techniques such as onlay bone grafting, guided bone regeneration (GBR) and distraction osteogenesis The study goal is to evaluate whether if there will be any benefit of using platelet rich fibrin (PRF) with the split crest technique regarding bone width gain and healing response in comparison with split crest technique alone, where PRF is considered an autologous, growth factor containing material which is easy to collect and is of low cost.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date June 1, 2019
Est. primary completion date March 15, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: 1. Patients with at least one missing tooth in the maxillary region 2. All the selected patients have a bucco-palatal width of the edentulous alveolar ridge from 3.5-5.5mm. 3. All the selected patients have at least 12 mm residual bone height at the edentulous area 4. The recipient site of the implant should be free from any pathological conditions. 5. No diagnosed bone disease or medication known to affect bone metabolism. 6. Patients who are cooperative, motivated, and hygiene conscious. Exclusion Criteria: 1. Patients unable to undergo minor oral surgical procedures. 2. Patients with a history of drug abuse or catabolic drugs. 3. Patients with a history of psychiatric disorder. 4. Patients with unrealistic expectations about the esthetic outcome of implant therapy. 5. Patients with insufficient vertical inter-arch space, upon centric occlusion, to accommodate the available restorative components. 6. Patients in the growth stage with partially erupted teeth. 7. Patients who have any systemic condition that may contraindicate implant therapy. 8. Patients who have any habits that might jeopardize the osseointegration process, such as smoking and alcoholism. 9. Patients with parafunctional habits that produce overload on the implant, such as bruxism and clenching.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Split Crest with PRF
Narrow ridges are split to increase the ridge width and immediate implants are placed with PRF closing the gap
Split Crest without PRF
Narrow ridges are split to increase the ridge width and immediate implants are placed without grafting

Locations

Country Name City State
Egypt Faculty of oral and dental medicine, Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone width gain 6 months
See also
  Status Clinical Trial Phase
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Completed NCT03897010 - Evaluation of Silica-calcium Phosphate Composite in Socket Augmentation Phase 4
Completed NCT03607006 - Ridge Augmentation Using Patient Specific PEEK Sheets vs. Autogenous Bone Shell Technique. N/A