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Efficacy of WJ-derived Mesenchymal Stem Cells in Combination With Parathyroid Hormone for Vertebral Compression Fracture

Efficacy of Wharton's Jelly-derived Mesenchymal Stem Cells in Combination With Parathyroid Hormone for Vertebral Compression Fracture

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05018637
Enrollment
30
Registered
2021-08-24
Start date
2020-09-01
Completion date
2022-12-31
Last updated
2021-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporotic Fractures, Vertebral Compression Fracture

Keywords

vertebral compression fracture, Back Pain

Brief summary

Osteoporotic vertebral compression fractures (OVCFs) are serious health problems. Transplantation of mesenchymal stem cells (MSCs) has gained considerable attention to treat osteoporosis and OVCFs because implanted healthy MSCs could be differentiated into osteoblasts and reduce the susceptibility of fractures by facilitating new bone formation. This study compares teriparatide (PTH 1-34) injection to combined treatment with Wharton's jelly-derived MSCs (WJ-MSCs) and teriparatide (PTH 1-34) in patients with OVCFs. It is a randomized, open-label, phase 2 study.

Interventions

DRUGWJ-MSC

Other: subcutaneous injection of 20 µg teriparatide once daily for 6 months, followed by oral administration of anti-resorptive drug for 6 months. Other: intramedullary injection of 4 x 107 WJ-MSCs (direct injection into the recently fractured vertebra) at baseline (day 0). subcutaneous injection of 20 µg teriparatide once daily for 6 months, followed by oral administration of anti-resorptive drug for 6 months.

DRUGTeriparatide

subcutaneous injection of 20 µg teriparatide once daily for 6 months, followed by oral administration of anti-resorptive drug for 6 months.

Sponsors

Inbo Han
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Postmenopausal women over 40 years of age * Compression fracture of the spine confirmed by MRI or bone scan * When the T score of the lumbar spine is less than -1.0 in the bone density test using DXA (Dual energy X ray absorptiometry) * Compression fracture is between 5th thoracic and 5th lumbar vertebra * When a new vertebral fracture occurs in less than 3 parts of the spine * Compression fracture of the spine within 6 weeks after minor trauma * Oswestry Disability Index (ODI) due to vertebral fracture is more than 30% * Back pain due to vertebral fracture has a Visual Analogue Scale (VAS) of 4 or higher. * In case of writing consent for stem cell transplantation therapy

Exclusion criteria

* Those who used osteoporosis treatment (bisphosphonate, selective estrogen receptor modulator, or parathyroid hormone) 6 months before the start of the clinical trial due to osteoporotic vertebral fracture. * In the case of inherited, metabolic, neoplastic, or infectious bone disease other than osteoporosis * Spinal fracture with neurological symptoms * Those who are taking drugs that affect bone metabolism such as steroids. * Those who have undergone spinal fixation surgery on the fracture site prior to the clinical trial * Those who have a history of psychiatry or who are currently undergoing treatment, who have judged that it is difficult to proceed with the clinical trial under the judgment of the researcher * Those who do not understand the purpose and method of this clinical trial as a study subject for drug or alcohol addiction * Those who participated in other clinical trials within 30 days prior to participation in the clinical trial * Those who may affect this clinical trial due to serious medical conditions (hypertension not controlled by drugs, diabetes not controlled by drugs, blood coagulation disease, cirrhosis, kidney failure, tumor) or immune deficiency * Factors less than 10 g/dL of hemoglobin in general blood test * If there is currently an acute systemic or local infection * Others who have clinically significant findings deemed inappropriate for this clinical trial due to medical judgment by the person in charge of the clinical trial * Those who are allergic to proteins required for cell production (fetal calf serum)

Design outcomes

Primary

MeasureTime frameDescription
improvement in Visual Analogue Scale12 monthsChange in the VAS at 1, 3, 6, 9, and 12 months after the transplantation of Wharton's jelly-derived MSCs (WJ-MSCs), compared to before the transplantation. on a scale of 0 to 10, with 0 meaning no pain and 10 meaning the worst pain you can imagine.

Secondary

MeasureTime frameDescription
improvement in Oswestry Disability Index12 monthsChange in the ODI at 1, 3, 6, 9, and 12 months after the transplantation of WJ-MSCs, compared to before the transplantation. on a scale of 0 to 3, with 0 meaning no disability and 10 meaning severe disability
Change in the T score (lumbar spine and femoral neck) of dual-energy x-ray absorptiometry12 monthsChange in the T score (lumbar spine and femoral neck) of dual-energy x-ray absorptiometry at 6 and 12 months after the transplantation compared to before the transplantation
Presence of new vertebral fracture12 monthsidentification of spine fracture based on x ray
Change in the bone mineral density (computed tomography) of fractured vertebrae12 monthsChange in the bone mineral density (computed tomography) at 6 and 12 months after the transplantation compared to before the transplantation

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026