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Treatment satisfaction by web survey for chronic spontaneous urticaria in Japan

Treatment satisfaction by web survey for chronic spontaneous urticaria in Japan - Treatment satisfaction survey for chronic spontaneous urticaria in Japan

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000047616
Enrollment
550
Registered
2022-05-02
Start date
2022-04-04
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

chronic spontaneous urticaria

Interventions

None listed

Sponsors

Sanofi K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Those who submit their informed consent and agree to participate in the survey - Those who stated that they have been diagnosed with chronic spontaneous urticaria or chronic urticaria by a physician in the past - Those who stated that their urticaria had continued more than 6 weeks with no trigger in the past - Those who have received some sort of treatment for chronic spontaneous urticaria or chronic urticaria within the past 3 months - Males and females who are 20 years old or older, reside in Japan, and can understand and answer the questionnaire in Japanese

Exclusion criteria

Exclusion criteria: - Correspond to an inappropriate answer

Design outcomes

Primary

MeasureTime frame
- Summary statistics (e.g., average) of TSQM-9 score - Correlation coefficient between TSQM-9 score and UCT/DLQI/Itch-NRS/Burning sensation NRS/Sleep NRS/SF-8/WPAI:GH score - TSQM-9 score by demographic characteristic - TSQM-9 score by treatment

Secondary

MeasureTime frame
- Summary statistics (e.g, average) of UCT/DLQI/SF-8/WPAI:GH scores - Responses to each NRS - Each score by demographic characteristic - Each score by treatment

Countries

Japan

Contacts

Public ContactYuko KISHI

Sanofi K.K. Dermatology Medical, Immunology Medical, Specialty Care

Sanofi_Medical@sanofi.com03-6301-4575

Outcome results

None listed

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