Reconstruction of Jaw Bone Using Mesenchymal Stem Cells
Primary Purpose
Bone Atrophy
Status
Completed
Phase
Phase 1
Locations
Norway
Study Type
Interventional
Intervention
BCP with autologous mesenchymal stem cells (MSC).
Sponsored by

About this trial
This is an interventional treatment trial for Bone Atrophy focused on measuring Mesenchymal stem cells, bone augmentation, bone regeneration
Eligibility Criteria
Inclusion Criteria:Patients presenting with an indication for an implant and wanting implant-borne prosthetic restoration.
- Patients presenting with lateral or vertical bone loss (focusing lateral bone loss) of the mandible behind the canine tooth.
- Lateral (width 5 mm or less) bone loss preventing the insertion of an implant without prior bone augmentation.
- Endentate for more than 6 months in the region requiring reconstruction.
- Endentate concerning at least 2 missing teeth in the region requiring reconstruction.
- Absence of clinical signs of infection in the region requiring reconstruction.
- Patients presenting with good dental hygiene (subjective criteria)
- Patients not presenting with any major oral pathologies.
- Dental crest size less than 5 mm.
General criteria:
- Adult patients over 18 and under 80 years of age.
- Patients in good general health presenting with a complete blood count and renal and hepatic function values within normal limits (confirmed by local laboratory tests).
- Patients with the capacity to understand medical information and give their informed consent.
Exclusion Criteria:
ocal criteria:
- Patients presenting with clinical or radiological signs of bone infection (acute or chronic osteomyelitis).
- Residual dentition close to the area requiring reconstruction with untreated endodontic disorder (apical granuloma or apical cyst).
- Untreated oral infection (cellulitis, periodontitis).
- Patients with poor hygiene (subjective criteria).
- Surgical procedure undertaken in the area requiring reconstruction less than 6 months prior to the bone graft.
- History of malignant tumors of the upper airways / digestive tract or of the jaw.
- History of or scheduled cervico-facial radiation therapy.
General criteria:
- The patient suffers from any serious coagulation disorders that could require substitution therapy
- The patient is receiving VKA therapy, which should be adjusted if necessary so that the INR does not exceed 2.5
- The patient has history of allergy to iodine or to local anesthetics(sulfites, etc.)., or a history of hematoma, or hemorrhage or blood coagulation disorders
- The patient has received localized iliac crest radiotherapy contraindicating withdrawal from the irradiated site
- The patient has major skin lesions or diseases.
- Patients presenting with bone metabolism disorders: hypophosphatemia, primary parathyroid osteitis or that is secondary to chronic renal insufficiency or osteomalacia, Paget's disease, vitamin D-related disorders, osteoporosis.
- Pregnant or breastfeeding women or women not using effective contraception if they are of childbearing age.
- Patients presenting with cancerous disorders (carcinoma, sarcoma, leukemia, lymphoma) or psychiatric disorders or with uncontrolled systemic diseases (diabetes, hypertension), or chronic renal disease.
- Severe bruxism.
- History of chemotherapy.
- Smoking or alcohol addiction. Occasional consumption of alcohol and/or smoking will be noted in the case report form.
- Patients with an ASA score of 0 or 1, incapable of tolerating general anesthesia.
- Immunosuppression
- Body mass index outside the normal range, particularly >30 because of increased surgical risk at the time of BM harvesting from the iliac crest.
- Risk of remote infection (orthopedic prosthesis implanted in the previous 6 months, patients presenting with a high risk of infective endocarditis, presence of pulmonary arteriovenous shunt, etc.).
- HIV, HTLV and/or syphilis seropositivity.
- Hepatitis B or C infection.
- Active autoimmune disease.
- History of immunosuppressant treatment or bone marrow treatment.
- Administration of treatment interfering with bone metabolism.
- Patients requiring antibiotic prophylaxis before any dental procedure
- Patients reticent to undergo dental care or periodontal treatment
- Concomitant treatments: history of treatment or current treatment with bisphosphonates, long term corticosteroid treatment.
Sites / Locations
- Institute of Clinical Dentistry, University of Bergen
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Augmentation of new alveolar bone
Arm Description
Augmentation of atrophied alveolar ridge with mesenchymal stem cells( MSC) and bis calcium phosphate(BCP)
Outcomes
Primary Outcome Measures
Amount of newly formed bone induced by MSCs and the bone substitute. These measurements are based on radiological assessments.
CBCT
Secondary Outcome Measures
Implant stability
Implant stability measurement using the Ostell system
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Safety of MSC in patients. Adverse events
Full Information
NCT ID
NCT02751125
First Posted
March 22, 2016
Last Updated
March 2, 2020
Sponsor
University of Bergen
Collaborators
University of Ulm, Haukeland University Hospital, Université de Nantes
1. Study Identification
Unique Protocol Identification Number
NCT02751125
Brief Title
Reconstruction of Jaw Bone Using Mesenchymal Stem Cells
Official Title
Jaw Bone Reconstruction Using a Combination of Autologous Mesenchymal Stem Cells and Biomaterial Prior to Dental Implant Placement
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
June 2014 (Actual)
Primary Completion Date
March 1, 2019 (Actual)
Study Completion Date
March 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bergen
Collaborators
University of Ulm, Haukeland University Hospital, Université de Nantes
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot study is aimed to reconstruct atrophied posterior alveolar mandibular ridges using biomaterial and autologous bone marrow derived stem cells (BMMSC) and to insert an implant into the new bone in a prosthetically guided position.
Detailed Description
Eleven patients presenting with the need of an implant retained restoration in the posterior mandibula and an alveolar ridge of maximum 4.5 mm width.
A clinical examination, x- rays and Cone Beam CT(CBCT) are accessed. A sample of the patients' bone marrow is extracted from the posterior alveolar ridge, immediately shipped to the collaborating good clinical practice (GCP) cell laboratory for cell expansion, and returned after 21 days. The stem cells mixed with Bi Calcium Phosphate (BCP) are then used to augment the alveolar ridge. The material is covered with a titanium reinforced membrane before closure of the site. After four to six months a bone biopsy is performed and implants are installed in the regenerated bone.
The patient will be followed after 1, 2, 3, and 5 years where implant stability will be assessed. Furthermore the new formed bone will be clinically and radiologically assessed at the same time.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Atrophy
Keywords
Mesenchymal stem cells, bone augmentation, bone regeneration
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Augmentation of new alveolar bone
Arm Type
Experimental
Arm Description
Augmentation of atrophied alveolar ridge with mesenchymal stem cells( MSC) and bis calcium phosphate(BCP)
Intervention Type
Drug
Intervention Name(s)
BCP with autologous mesenchymal stem cells (MSC).
Other Intervention Name(s)
MSC and BCP
Intervention Description
Augmentation of narrow alveolar ridge with BCP and MSC
Primary Outcome Measure Information:
Title
Amount of newly formed bone induced by MSCs and the bone substitute. These measurements are based on radiological assessments.
Description
CBCT
Time Frame
Four to six months post augmentation
Secondary Outcome Measure Information:
Title
Implant stability
Description
Implant stability measurement using the Ostell system
Time Frame
12 months
Title
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Description
Safety of MSC in patients. Adverse events
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:Patients presenting with an indication for an implant and wanting implant-borne prosthetic restoration.
Patients presenting with lateral or vertical bone loss (focusing lateral bone loss) of the mandible behind the canine tooth.
Lateral (width 5 mm or less) bone loss preventing the insertion of an implant without prior bone augmentation.
Endentate for more than 6 months in the region requiring reconstruction.
Endentate concerning at least 2 missing teeth in the region requiring reconstruction.
Absence of clinical signs of infection in the region requiring reconstruction.
Patients presenting with good dental hygiene (subjective criteria)
Patients not presenting with any major oral pathologies.
Dental crest size less than 5 mm.
General criteria:
Adult patients over 18 and under 80 years of age.
Patients in good general health presenting with a complete blood count and renal and hepatic function values within normal limits (confirmed by local laboratory tests).
Patients with the capacity to understand medical information and give their informed consent.
Exclusion Criteria:
ocal criteria:
Patients presenting with clinical or radiological signs of bone infection (acute or chronic osteomyelitis).
Residual dentition close to the area requiring reconstruction with untreated endodontic disorder (apical granuloma or apical cyst).
Untreated oral infection (cellulitis, periodontitis).
Patients with poor hygiene (subjective criteria).
Surgical procedure undertaken in the area requiring reconstruction less than 6 months prior to the bone graft.
History of malignant tumors of the upper airways / digestive tract or of the jaw.
History of or scheduled cervico-facial radiation therapy.
General criteria:
The patient suffers from any serious coagulation disorders that could require substitution therapy
The patient is receiving VKA therapy, which should be adjusted if necessary so that the INR does not exceed 2.5
The patient has history of allergy to iodine or to local anesthetics(sulfites, etc.)., or a history of hematoma, or hemorrhage or blood coagulation disorders
The patient has received localized iliac crest radiotherapy contraindicating withdrawal from the irradiated site
The patient has major skin lesions or diseases.
Patients presenting with bone metabolism disorders: hypophosphatemia, primary parathyroid osteitis or that is secondary to chronic renal insufficiency or osteomalacia, Paget's disease, vitamin D-related disorders, osteoporosis.
Pregnant or breastfeeding women or women not using effective contraception if they are of childbearing age.
Patients presenting with cancerous disorders (carcinoma, sarcoma, leukemia, lymphoma) or psychiatric disorders or with uncontrolled systemic diseases (diabetes, hypertension), or chronic renal disease.
Severe bruxism.
History of chemotherapy.
Smoking or alcohol addiction. Occasional consumption of alcohol and/or smoking will be noted in the case report form.
Patients with an ASA score of 0 or 1, incapable of tolerating general anesthesia.
Immunosuppression
Body mass index outside the normal range, particularly >30 because of increased surgical risk at the time of BM harvesting from the iliac crest.
Risk of remote infection (orthopedic prosthesis implanted in the previous 6 months, patients presenting with a high risk of infective endocarditis, presence of pulmonary arteriovenous shunt, etc.).
HIV, HTLV and/or syphilis seropositivity.
Hepatitis B or C infection.
Active autoimmune disease.
History of immunosuppressant treatment or bone marrow treatment.
Administration of treatment interfering with bone metabolism.
Patients requiring antibiotic prophylaxis before any dental procedure
Patients reticent to undergo dental care or periodontal treatment
Concomitant treatments: history of treatment or current treatment with bisphosphonates, long term corticosteroid treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cecilie Gjerde, DDS
Organizational Affiliation
University of Bergen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Clinical Dentistry, University of Bergen
City
Bergen
State/Province
Hordaland
ZIP/Postal Code
5008
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30092840
Citation
Gjerde C, Mustafa K, Hellem S, Rojewski M, Gjengedal H, Yassin MA, Feng X, Skaale S, Berge T, Rosen A, Shi XQ, Ahmed AB, Gjertsen BT, Schrezenmeier H, Layrolle P. Cell therapy induced regeneration of severely atrophied mandibular bone in a clinical trial. Stem Cell Res Ther. 2018 Aug 9;9(1):213. doi: 10.1186/s13287-018-0951-9.
Results Reference
result
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Reconstruction of Jaw Bone Using Mesenchymal Stem Cells
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