Validation of Hidrex iontophoresis (conceptION) with regard to its user acceptance and effectiveness in patients with hyperhidrosis

Validation of Hidrex iontophoresis (conceptION) with regard to its user acceptance and effectiveness in patients with hyperhidrosis - Ion2Effect

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035943

Enrollment

100

Registered

2025-02-13

Start date

2025-01-13

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

R61

Interventions

Group 1: Users of the Hidrex iontophoresis device conceptION who have given their consent to be contacted in writing for study purposes and who have used the conceptION at least 14 times are surveyed

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Presence of hyperhidrosis, use of the Hidrex iontophoresis device conceptION, proficiency in German, presence of a signed declaration of consent

Exclusion criteria

Exclusion criteria: Non-fulfilment of the inclusion criteria

Design outcomes

Primary

Measure	Time frame
Assessment of user acceptance and (self-reported) effectiveness of Hidrex Iontophoresis using conceptION in patients with hyperhidrosis	—

Countries

Germany

Contacts

Public ContactSwen Malte John

Abteilung "Dermatologie, Umweltmedizin, Gesundheitstheorie" Universität Osnabrück Institut für interdisziplinäre Dermatologische Prävention und Rehabilitation (iDerm) an der Universität Osnabrück

johnderm@uos.de+49541-969-2357

Outcome results

None listed

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