A Non-Interventional Study to Compare Digital Monitoring of Patients with chronic spontaneous urticaria by Telemedicine to Face-to-Face Visits in Germany

A Non-Interventional Study to Compare Digital Monitoring of Patients with chronic spontaneous urticaria by Telemedicine to Face-to-Face Visits in Germany - DigiMoc

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00036732

Enrollment

200

Registered

2025-04-29

Start date

2024-06-11

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

L50.9

Interventions

Group 1: Telemedicine Group 2: Face to Face visits

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Written informed consent for participation obtained from the subject Diagnosed chronic spontaneous urticaria Medical therapy for CSU Concomitant chronic inducible urticaria is allowed Willing and be able to perform digital visits

Exclusion criteria

Exclusion criteria: simultaneous participation in any clinical trial

Design outcomes

Primary

Measure	Time frame
To quantitatively describe the frequency of UCT usage in CSU patients monitored via teledermatology compared to F2F visits.	—

Secondary

Measure	Time frame
To quantitatively describe the type and number of physician- patient interaction in both arms.	—

Countries

Germany

Contacts

Public ContactAlexander Zink

Klinikum rechts der Isar

alexander.zink@tum.de+49 89 4140 3038

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026