Skip to content

Therapeutic effect on disodium pamidronate administration to diffuse sclerosing mandible osteomyelitis

Therapeutic effect on disodium pamidronate administration to diffuse sclerosing mandible osteomyelitis - On the effect of disodium pamidronate on diffuse curable mandibular osteomyelitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000033725
Enrollment
5
Registered
2020-10-01
Start date
2020-10-01
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

diffuse sclerosing osteomyelitis

Interventions

None listed

Sponsors

Department of Oral and Maxillofacial Surgery, Osaka Medical and Pharmaceutical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who underwent dental oral surgery at Osaka Medical University Hospital and underwent treatment with diamantane pamidronate for DSO

Exclusion criteria

Exclusion criteria: Patients who did not obtain consent to this study

Design outcomes

Primary

MeasureTime frame
Dissolve pamidronate disodium in 500ml of raw diet for patients with diffuse osteomyelitis and take IV infusion over 4 hours. The number of doses is only once, but when symptoms such as pain are observed, re-administration is performed at intervals of 3 to 6 months.Comparison of changes in jaw bone due to clinical symptoms and image findings before and after administration of disodium pamidronate, and evaluate the improvement effect of diamid pamidronate on DSO

Countries

Japan

Contacts

Public ContactNakajima Yoichiro

Osaka Medical and Pharmaceutical University Department of Oral and Maxillofacial Surgery

n4160@ompu.ac.jp0726831221

Outcome results

None listed

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