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Improvement in pain and function through analgesic and anti-inflammatory radiotherapy in patients with finger arthritis, medial/lateral epicondylitis or plantar fasciitis

Improvement in pain and function through analgesic and anti-inflammatory radiotherapy in patients with finger arthritis, medial/lateral epicondylitis or plantar fasciitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00006288
Enrollment
150
Registered
2014-07-09
Start date
2013-01-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

plantar fasciitis, epicondylitis, polyarthritis of the finger joints M15.9 M19.9 M18 M76 M77.0 M77.1 M77.3 M77.5 M77.9

Interventions

Group 1: Analgesic and anti-inflammatory Radiotherapy. Radiotherapy is given twice a week for eight treatments, i.e. over 4 weeks. Each treatment lasts 10 – 15 minutes. The clinical assessments will b

Sponsors

Kantonsspital AarauZentrum für Radio-Onkologie KSA-KSB
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 40 year, Karnofsky Index at least 70%, Patients cannot be pregnant, Patients of child bearing age must use a medically acceptable form of contraception during the radiotherapy as well as 12 months after, Patients cannot have any congenital disease with increased sensitivity to radiation, absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial, before patient registration/randomization, written informed consent must be given according to ICH/GCP, and national/local regulations, patients will have been treated with conventional therapeutic interventions for at least 6 months

Exclusion criteria

Exclusion criteria: congenital disease with increased sensitivity to radiation, psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule

Design outcomes

Primary

MeasureTime frame
Pain will be assessed using the Visual Analog Scale. Musculoskeletal function will be documented using a dynamometer for patients with hand and elbow disorders and a walking test will be performed for patients with plantar fasciitis. The HAQ (health assessment) and EQ-5D (quality of life) questionnaires will be completed by all patients. Assessments will be performed at baseline and at 2, 6 and 12 months after radiotherapy.

Countries

Switzerland

Contacts

Public ContactSusanne Desborough

Kantonsspital Aarau AGZentrum für Radio-Onkologie KSA-KSB

susanne.desborough@ksa.ch+41628385408

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026