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Observational study of tin splint for Heberden's nodule

Observational study of tin splint for Heberden's nodule - Observational study of tin splint

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000026637
Enrollment
50
Registered
2017-04-01
Start date
2016-05-18
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

Heberden&#39

Interventions

Frequency or duration of use was not specified, and patients were told to wear or remove the splints freely depending on the severity of their pain.

Sponsors

Kanazawa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients with painful Hebreden's nodule.

Exclusion criteria

Exclusion criteria: patients with secondary joint deformation due to comorbid conditions such as trauma, gout, or rheumatoid arthritis, and those with severe deformations with joint subluxation were excluded from the study.

Design outcomes

Primary

MeasureTime frame
numeric pain scale—

Countries

Japan

Contacts

Public ContactKaoru Tada

Kanazawa University Department of orthopaedic surgery

tdkr@med.kanazawa-u.ac.jp0762652000

Outcome results

None listed

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