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Inhibitory effect of teriparatide in knee osteoarthritis

Study on inhibitory effect of teriparatide in knee osteoarthritis - PTH on OA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs051180095
Enrollment
60
Registered
2019-03-06
Start date
2018-10-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Knee osteoarthritis, osteoporosis Knee OA

Interventions

Arm A: Weekly treatment of teriparatide (56.5 micro g) for 24 months. Arm B: Daily treatment f Vitamin D3 analog 0.25, 0.5, 0.75 or 1.0 micro g) for 24 months.

Sponsors

Matsuda Shuichi
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patient who was diagnosed as osteoporosis with high risk of fracture Patient who was diagnosed as osteoarthritis of the knee with Kellgren-Lawrence grade 2 or 3. Patient who has knee pain.

Exclusion criteria

Exclusion criteria: Patient who uses corticosteroid The reason of the pain is other than osteoarthritis Patient with dementia Patient who has contraindication for the drug which is used in this study.

Design outcomes

Primary

MeasureTime frame
Disease progression by X ray (bone trabecular integrity, Joint space narrowing, width)

Secondary

MeasureTime frame
Cartilage volume by MRI, Grade of osteoarthritis by Xray (Kellgren-Lawrence grade) Clinical outcomes (WOMAC, KSS)

Contacts

Public ContactKohei Nishitani

Kyoto University Hospital

nkohei@kuhp.kyoto-u.ac.jp+81-75-751-3366

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026