Reconstruction of Jaw Bone Using Mesenchymal Stem Cells

Phase 1

Completed

• Conditions: Bone Atrophy
• Interventions: Drug: BCP with autologous mesenchymal stem cells (MSC).

• Registration Number: NCT02751125
• Lead Sponsor: University of Bergen

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.

Study Timeline

• Study Start: 2014-06
• Study First Submitted: 2016-03-22
• Study First Submitted QC: 2016-04-25
• Study First Posted: 2016-04-26
• Primary Completion: 2019-03-01
• Status Verified: 2020-03
• Study Completion: 2020-03-01
• Last Update Submitted: 2020-03-02
• Last Update Posted: 2020-03-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 13

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Augmentation of new alveolar bone	BCP with autologous mesenchymal stem cells (MSC).	Augmentation of atrophied alveolar ridge with mesenchymal stem cells( MSC) and bis calcium phosphate(BCP)

Primary Outcome Measures

Name	Time	Method
Amount of newly formed bone induced by MSCs and the bone substitute. These measurements are based on radiological assessments.	Four to six months post augmentation	CBCT

Secondary Outcome Measures

Name	Time	Method
Implant stability	12 months	Implant stability measurement using the Ostell system
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]	5 years	Safety of MSC in patients. Adverse events

Trial Locations

Locations (1)

Institute of Clinical Dentistry, University of Bergen; 🇳🇴 Bergen, Hordaland, Norway