An interventional study of autogenous bone and Mineralized plasmatic matrix in Bone Resorption, sponsored by Cairo University. Status unknown. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-01-09.
Sponsored by Cairo University · Not applicable, Interventional, and Treatment
Using growth factors obtained from patient's venous blood mixed with particulate autogenous bone the study compares bone gain by implant with gold standards in sinus Lift procedures for future implant insertion.
To study the effectiveness of MPM in ridge augmentation with implant insertion compared with autogenous bone graft.
-PICO Population(P) : Patients with defective posterior maxillary alveolar ridge. Intervention (I) :Implant placement and ridge augmentation with MPM. Comparator (C) : Autogenous bone graft. Outcome (O) : Patient satisfaction - Implant stability.
153 studies on the registry are indexed under Bone Resorption; 25 are open to participants now.
This study's planned enrollment of 20 is close to the median of 22 across 133 interventional studies indexed under Bone Resorption.
Browse Bone Resorption studies →Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.
Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Patients with defective posterior maxillary alveolar ridges requiring implant insertion will have Autogenous bone graft (Gold standard) and to be used for bone augmentation with sinus lift.
Other: autogenous bone
Patients with defective posterior maxillary alveolar ridges requiring implant insertion will receive bone graft using Mineralized plasmatic matrix.
Other: Mineralized plasmatic matrix
Autogenous bone graft (gold standard). sinus lift with autogenous bone.
Also known as: Autobone
By using venoud blood from the patient, together with bone graft, a centrifuge will be used to obtain the top layer after centrifuging blood at 3000 RPM.
Also known as: MPM
Patient Satisfaction regarding aesthetic results will be measured using questionnaire.
outcome will be measure using questionnaire.
Time frame: 9 months
Stability of dental implants.
will be measured using OSTELL Device.
Time frame: 5 months
No study locations are listed for this record.
Plan to share: No — Evaluation of the comparative Effectiveness of MPM Augmentation in posterior maxillary ridge defects with Autogenous bone graft.
No publications or documents are linked to this record.
This study is status unknown, as verified in Dec 2016. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Cairo University