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Clinical trial of efficacy and safety as a pilot study in pachydermoperiostosis

Clinical trial of efficacy and safety as a pilot study in pachydermoperiostosis - A pilot study in PDP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022397
Enrollment
3
Registered
2016-05-21
Start date
2016-01-18
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

pachydermoperiostosis

Interventions

Medicine A 200 mg, twice daily, for 1 year

Sponsors

National Center for Child Health and Development
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)A patient having clinical triad and excluded the following conditions: secondary hypertrophic osteoarthropathy, systemic bone diseases, acromegaly, Graves' disease-associated osteoarthropathy (thyroid acropachy, EMO syndrome) (2)A patient who was found to have gene mutations in the HPGD or SLCO2A1 gene (3)A patient who MR imaging in brain and legs and X-ray photograph in extremities were taken.

Exclusion criteria

Exclusion criteria: Patients who met the following conditions were excluded: (1)allergy to Medicine A, (2)history of asthma, (3)history of gastrointestinal ulcer or bleeding, (4)renal diseases (serum creatinine concentration more than 1.2 mg/dl, including having a history of dialysis), (5)liver dysfunction (serum alanine or aspartate transaminase concentrations more than 3 times the upper limit of normal range), (6)heart failure or myocardial infarction, (7)body weight less than 40 kg.

Design outcomes

Primary

MeasureTime frame
clinical symptoms and signs

Secondary

MeasureTime frame
serum/urinary PGE2 content

Countries

Japan

Contacts

Public ContactMayumi Sako

National Center for Child Health and Development Division for Clinical Trials

sako-m@ncchd.go.jp+81-3-3416-0181

Outcome results

None listed

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