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CompletedNCT00722189Updated Jun 9, 2023

Observational Study of Efficacy and Safety of Travogen Cream and Travocort Cream in the Treatment of Mycoses

An observational study in Skin Mycoses, sponsored by LEO Pharma. Completed at 1 site in Russian Federation. Per ClinicalTrials.gov, last updated 2023-06-09.

Sponsored by LEO Pharma · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
900
Sex
All
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Study summary

An assessment of the efficacy and safety of Travogen cream and Travocort cream in the treatment of local skin mycoses

02

Conditions studied

  • Skin Mycoses

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Keywords

  • Mycoses
03

In context

Mycoses

539 studies on the registry are indexed under Mycoses; 55 are open to participants now.

This study's enrollment of 900 is above the median of 152 across 150 observational studies indexed under Mycoses.

Browse Mycoses studies →

Lead sponsor

LEO Pharma is the lead sponsor of 221 studies on the registry; 5 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 24 (77%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with diagnosed skin mycoses

Inclusion criteria

  • Diagnosis of skin mycosis

Exclusion criteria

Exclusion Criteria:

  • Allergies to study medication
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
900 participants (actual)

Groups and cohorts

  • A

    All patients treated

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What researchers measure

Primary outcomes

  1. Efficacy of Travogen / Travocort in the treatment of skin mycoses / Travogen Cream and Travocort Cream will be prescribed by a physician

    Time frame: Baseline to end of study

Secondary outcomes

  1. Patient satisfaction

    Time frame: Baseline to end of study

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Study locations

1 site
  • Kashkin Clinical Research Mycological Institute
    St Petersburg, Russian Federation
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00722189
Lead sponsor
LEO Pharma
Collaborators
Bayer
Responsible party
Sponsor
First posted
Jul 25, 2008
Start date
Jul 2008
Primary completion
Jan 2009
Completion
Feb 2009
Last update
Jun 9, 2023

Study contacts

Bayer Study Director
study director · Bayer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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Discussion

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