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Does local application of betamethasonvalerate 0.1% cream twice a day reduce the complaints of chronic chilblains?

Does local application of betamethasonvalerate 0.1% cream twice a day reduce the complaints of chronic chilblains? - BCCC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34743
Enrollment
50
Registered
2009-12-24
Start date
2010-06-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Chronic Chilblains

Interventions

The intervention which is compared to the placebo consists of the thin application of betamethasonvaleraat cream 0,1 % twice a day for 6 weeks where the perniones laesions are located .

Sponsors

Huisartspraktijk Souwer
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 18 years or older; able to understand and follow instructions; Complaints of chronic pernio for at least 3 weeks at inclusion: itching or painfull blue-red discolorated laesions at fingers and/or toes, other lokalisations at the feet or lateral side of the thigs ("the Kibes"). The laesions may be swollen ans ulceration may be pressent but not obligitory. Onset of complaints is in the period november to februari.

Exclusion criteria

Exclusion criteria: Known inflamatory disease (RA, SLE et cetera); pregnancy; lactation; actual use of a calcium antagonist, use of corticosteroïd containing cream in the past four weeks, skin defects at the skinparts to treat.

Design outcomes

Primary

MeasureTime frame
We consider the intervention effective if a reduction of the experienced complaints or is discovered, displayed in a decline of the score "complaint" with at least 10 mm on the visual analogue scale concerned. "Complaint" is defind as Max (itch,pain): the Vas score for or itch or pain, depending on the highest score.

Secondary

MeasureTime frame
Secondary we register scores for impairement and the experienced side effects, skin irritation, and symptoms of skin atrophy: purpurae, inclination to bleed and depigmentation.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)