About this trial
The purpose of this trial is to evaluate if the use of Bone Morphogenic Protein(BMP)/Demineralized Bone Matrix (DBM) versus the use of autologous Iliac Crest Bone Graft (ICBG) will result in an increase in total cost effectiveness for patients undergoing alveolar bone graft (ABG) for Cleft Lip and Palate (CLP) and to see if patients who are treated with DBM/BMP will have reduced post-operative pain scores,reduced operative times,and similar rates of bone healing compared to conventional ICBG.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patient with CLP(unilateral or bilateral)
Radiographically evident open bone defect of the alveolus
Dentition evaluated by orthodontist and cleared for ABG surgery
Disqualifiers
Patients without CLP
Previous failed repair of alveolar cleft
Patients who have previously undergone successful ABG
Patients without an alveolar defect
Trial design
Parallel
Treatments tested in this trial
Intervention group (DBM/BMP)
DrugAll patients will undergo a standard procedure for exposure of the cleft alveolar defect and closure of all oronasal fistulae. After induction of general anesthesia, the patient will be intubated with an oral ray tube and prepped and draped in sterile fashion. Pre-operative antibiotics will be given to cover oral flora (i.e. Unasyn or clindamycin if penicillin allergy exists). The intra-oral space will be exposed and the nasal floor and palatal mucosa will be primarily closed to create a water-tight space for the graft. The integrity of the nasal floor mucosa will be tested using methylene blue dye. Following closure of the fistula, the alveolar bone graft will be performed. For the treatment group, 10cc of crushed DBM will be mixed with the micro-sized sponge of rh-BMP-2 (Infuse Bone Graft, Medronic, Minneapolis, MN). The sponge and DBM will then be packed into the defect to completely fill the bony space (FIGURE 3). The anterior mucosa will then be closed.
Control group(autologous ICBG)
DrugThe patient will be induced with anesthesia, prepped, and draped. The intra-oral space will be exposed and the nasal floor and palatal mucosa will be primarily closed to create a water-tight space for the graft. The integrity of the nasal floor mucosa will be tested using methylene blue dye. Following closure of the fistula, the alveolar bone graft will be performed.In the control group, the ICBG will be harvested percutaneously using the Accumed bone graft harvesting system. Briefly, an incision will be made in iliac crest and drill bit inserted. Multiple passes of the drill be used to harvest as much autograft bone as possible from the cancellous region of the iliac crest.Following harvest, fibrin glue will be instilled for hemostasis and a Ropivicaine On-Q pain pump inserted for post-operative pain control. The harvest bone graft will be packed into the alveolar defect in a similar fashion and the mucosa closed anteriorly.
Treatment groups
Trial outcomes
Primary outcomes
Health system costs per successful bone graft.
Health system costs will be reported as the total sum of all costs including incremental surgeon time costs, hospital costs, revision costs, and additional outpatient costs for clinic or ER visits. Bone graft success be defined as no need for a repeat bone graft, as well as by assessment by blinded orthodontist evaluations of the Post op Cone beam computed tomography(CBCT).
Secondary outcomes
Graft Success
Graft success as indicated by number of patients that did not have exposure of graft as assessed by post op CBCT
Infection
Graft success as indicated by number of patients that had no graft infection as assessed by post op CBCT
Fistula Recurrence
Graft success as indicated by number of patients that had no recurrence of oronasal fistula as assessed by post op CBCT
Rate of Revision ABG
Graft success as indicated by number of patients that had no no need for repeat bone graft as assessed by post op CBCT
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